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                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1410
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1418] => Array
                                                        (
                                                            [id] => 1418
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 385
                                                            [name] => d) Ocenę ryzyka przekazania niepłodności potomstwu płci żeńskiej
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1411
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [386] => Array
                                        (
                                            [id] => 386
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Wskaż zdanie prawdziwe:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1419] => Array
                                                        (
                                                            [id] => 1419
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 386
                                                            [name] => a) CBAVD jest wynikiem mutacji tylko w genie CFTR
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1412
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1420] => Array
                                                        (
                                                            [id] => 1420
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 386
                                                            [name] => b) Premutacje genu FMR1 są przyczyną przedwczesnego wygasania funkcji jajników
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1413
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1421] => Array
                                                        (
                                                            [id] => 1421
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 386
                                                            [name] => c) Jednym ze wskazań do badania genu CFTR jest występowanie CBAVD z towarzyszącą agenezją nerki
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1414
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1422] => Array
                                                        (
                                                            [id] => 1422
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 386
                                                            [name] => d) Prawidłowy wynik kariotypu, analizy regionu AZF chromosomu Y i genu CFTR oznacza, że przyczyną oligozoospermii u Pacjenta nie jest czynnik genetyczny.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1415
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [387] => Array
                                        (
                                            [id] => 387
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Zaznacz odpowiedź prawidłową dotyczącą techniki MLPA wykorzystywanej w szybkiej diagnostyce aneuploidii u płodu:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1423] => Array
                                                        (
                                                            [id] => 1423
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 387
                                                            [name] => a) wykrywa aberracje zrównoważone, nie wykrywa kontaminacji krwią matczyną
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1416
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1424] => Array
                                                        (
                                                            [id] => 1424
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 387
                                                            [name] => b) nie wykrywa kontaminacji krwią matczyną, nie wykrywa mozaikowości, nie wykrywa triploidii
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1417
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1425] => Array
                                                        (
                                                            [id] => 1425
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 387
                                                            [name] => c) wykrywa aberracje zrównoważone, wykrywa triploidię
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1418
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1426] => Array
                                                        (
                                                            [id] => 1426
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 387
                                                            [name] => d) wykrywa triploidię, nie wykrywa aberracji zrównoważonych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1419
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [388] => Array
                                        (
                                            [id] => 388
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Które zdania NIE dotyczą zespołu Klinefeltera:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1427] => Array
                                                        (
                                                            [id] => 1427
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 388
                                                            [name] => a) jest najczęstszą genetyczną przyczyną niepłodności męskiej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1420
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1428] => Array
                                                        (
                                                            [id] => 1428
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 388
                                                            [name] => b) związany jest z azoospermią lub znaczną oligozoospermią
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1421
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1429] => Array
                                                        (
                                                            [id] => 1429
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 388
                                                            [name] => c) zazwyczaj stwierdza się kariotyp mozaikowy
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1422
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1430] => Array
                                                        (
                                                            [id] => 1430
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 388
                                                            [name] => d) występuje z częstością 1 na 500 mężczyzn
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1423
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [133] => Array
                                        (
                                            [id] => 133
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => W dziedziczeniu autosomalnym recesywnym: 1. Rodzice najczęściej są nosicielami mutacji w genie związanym z chorobą dziecka. 2. Rodzice nosiciele ponoszą ryzyko wynoszące 25% wystąpienia choroby u kolejnego potomstwa. 3. Nosiciel mutacji w jednym allelu genu jest osobą zdrową. 4. Osoba z chorobą o uwarunkowaniu autosomalnym recesywnym ma szanse na zdrowe potomstwo, jeśli u partnera zostanie wykluczone nosicielstwo mutacji w genie związanym z chorobą. 5. Pokrewieństwo zwiększa ryzyko wystąpienia choroby o tym uwarunkowaniu genetycznym. Odpowiedź prawidłowa to:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [443] => Array
                                                        (
                                                            [id] => 443
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 133
                                                            [name] => a. tylko 2
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 436
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [444] => Array
                                                        (
                                                            [id] => 444
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 133
                                                            [name] => b. 1, 2, 3
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 437
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [445] => Array
                                                        (
                                                            [id] => 445
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 133
                                                            [name] => c. 2, 3, 5
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 438
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [446] => Array
                                                        (
                                                            [id] => 446
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 133
                                                            [name] => Wszystkie odpowiedzi są prawdziwe
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 439
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [389] => Array
                                        (
                                            [id] => 389
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Zaznacz BŁĘDNE zdanie dotyczące chromosomów markerowych stwierdzanych u osób z niepłodnością
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1431] => Array
                                                        (
                                                            [id] => 1431
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 389
                                                            [name] => a) Najczęściej stwierdza się markery pochodzące z chromosomów akrocentrycznych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1424
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1432] => Array
                                                        (
                                                            [id] => 1432
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 389
                                                            [name] => b) Chromosomy markerowe wpływają na niepowodzenia rozrodu nosicieli, ponieważ zawierają geny związane z niepłodnością
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1425
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1433] => Array
                                                        (
                                                            [id] => 1433
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 389
                                                            [name] => c) U osób niepłodnych najczęściej stwierdza się markery pochodzące z chromosomu 15.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1426
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1434] => Array
                                                        (
                                                            [id] => 1434
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 389
                                                            [name] => d) Obecność chromosomu markerowego zaburza proces gametogenezy
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1427
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [134] => Array
                                        (
                                            [id] => 134
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Zaznacz odpowiedź prawdziwą: 1. Na podstawie analizy rodowodu nie można podejrzewać sposobu dziedziczenia choroby. 2. W chorobach o dziedziczeniu sprzężonym z chromosomem X recesywnym u matek nosicielek choroby może nie być żadnych objawów klinicznych, a chorują wyłącznie synowie. 3. W chorobach o uwarunkowaniu autosomalnym dominującym osoba chora ponosi ryzyko wynoszące 100% wystąpienia choroby u potomstwa. 4. W chorobach o dziedziczeniu sprzężonym z chromosomem X dominującym chorują wyłącznie kobiety, ponieważ najczęściej są one letalne dla płci męskiej. Odpowiedź prawidłowa to:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [447] => Array
                                                        (
                                                            [id] => 447
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 134
                                                            [name] => a. 1, 3
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 440
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [448] => Array
                                                        (
                                                            [id] => 448
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 134
                                                            [name] => b. 1, 2, 3
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 441
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [449] => Array
                                                        (
                                                            [id] => 449
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 134
                                                            [name] => c. 2, 4
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 442
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [450] => Array
                                                        (
                                                            [id] => 450
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 134
                                                            [name] => d. 2, 3, 4
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 443
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [390] => Array
                                        (
                                            [id] => 390
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Aby ustalić typ trisomii (prosta czy translokacyjna) należy wykonać badanie:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1435] => Array
                                                        (
                                                            [id] => 1435
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 390
                                                            [name] => a) QF-PCR
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1428
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1436] => Array
                                                        (
                                                            [id] => 1436
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 390
                                                            [name] => b) Rapid FISH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1429
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1437] => Array
                                                        (
                                                            [id] => 1437
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 390
                                                            [name] => c) MLPA
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1430
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1438] => Array
                                                        (
                                                            [id] => 1438
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 390
                                                            [name] => d) Kariotyp
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1431
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [135] => Array
                                        (
                                            [id] => 135
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Zespół Crouzona: 1. Należy do zespołów kraniostenoz. 2. Występuje w tym zespole przedwczesne zarastanie szwów czaszkowych. 3. Charakteryzuje się brakiem występowania wad kończyn i wad innych narządów poza nieprawidłowościami budowy czaszki. 4. Brak kraniostenozy nie wyklucza rozpoznania tego zespołu. Odpowiedź prawidłowa to:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [451] => Array
                                                        (
                                                            [id] => 451
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 135
                                                            [name] => a. Tylko 1
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 444
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [452] => Array
                                                        (
                                                            [id] => 452
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 135
                                                            [name] => b. 1 i 2
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 445
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [453] => Array
                                                        (
                                                            [id] => 453
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 135
                                                            [name] => c. 2 i 3
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 446
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [454] => Array
                                                        (
                                                            [id] => 454
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 135
                                                            [name] => d. Wszystkie odpowiedzi są prawidłowe
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 447
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [391] => Array
                                        (
                                            [id] => 391
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Zaznacz BŁĘDNE zdanie:
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                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1439] => Array
                                                        (
                                                            [id] => 1439
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 391
                                                            [name] => a) Wszystkie kobiety ciężarne powinny mieć zaproponowane przesiewowe badania prenatalne
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1432
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1440] => Array
                                                        (
                                                            [id] => 1440
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 391
                                                            [name] => b) Badania inwazyjne powinny być wykonane po uprzednich badaniach przesiewowych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1433
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1441] => Array
                                                        (
                                                            [id] => 1441
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 391
                                                            [name] => c) Badania przesiewowe nie określają ryzyka wystąpienia aberracji chromosomowych
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1434
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1442] => Array
                                                        (
                                                            [id] => 1442
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 391
                                                            [name] => d) Kobietom, które decydują się na pominięcie etapu skriningowego, należy umożliwić wykonanie badania inwazyjnego po uprzednim poinformowaniu o możliwych powikłaniach
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1435
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [136] => Array
                                        (
                                            [id] => 136
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Metody cytogenetyczne umożliwiające analizę całego genomu to:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [455] => Array
                                                        (
                                                            [id] => 455
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 136
                                                            [name] => a. FISH i aCGH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 448
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [456] => Array
                                                        (
                                                            [id] => 456
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 136
                                                            [name] => b. MLPA i kariotyp
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 449
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [457] => Array
                                                        (
                                                            [id] => 457
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 136
                                                            [name] => c. kariotyp i aCGH
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 450
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [458] => Array
                                                        (
                                                            [id] => 458
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 136
                                                            [name] => d. MLPA i FISH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 451
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [392] => Array
                                        (
                                            [id] => 392
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Które czynniki genetyczne należą do najczęstszych przyczyn niepowodzeń ciąży?
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1443] => Array
                                                        (
                                                            [id] => 1443
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 392
                                                            [name] => a) choroby jednogenowe zarodka/płodu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1436
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1444] => Array
                                                        (
                                                            [id] => 1444
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 392
                                                            [name] => b) disomia jednorodzicielska
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1437
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1445] => Array
                                                        (
                                                            [id] => 1445
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 392
                                                            [name] => c) aberracje chromosomowe
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1438
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1446] => Array
                                                        (
                                                            [id] => 1446
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 392
                                                            [name] => d) polimorfizmy i mutacje w genach, związane z różnymi procesami zachodzącymi w komórkach, takimi jak na przykład: immunosupresja, apoptoza, angiogeneza, czy przekazywanie sygnałów w komórce.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1439
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [137] => Array
                                        (
                                            [id] => 137
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Które z metod pozwalają na identyfikację translokacji zrównoważonych?
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [459] => Array
                                                        (
                                                            [id] => 459
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 137
                                                            [name] => a. kariotyp i FISH
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 452
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [460] => Array
                                                        (
                                                            [id] => 460
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 137
                                                            [name] => b. kariotyp i aCGH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 453
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [461] => Array
                                                        (
                                                            [id] => 461
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 137
                                                            [name] => c. aCGH i MLPA
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 454
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [462] => Array
                                                        (
                                                            [id] => 462
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 137
                                                            [name] => d. FISH i MLPA
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 455
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [393] => Array
                                        (
                                            [id] => 393
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Zaznacz PRAWIDŁOWE zdanie:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1447] => Array
                                                        (
                                                            [id] => 1447
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 393
                                                            [name] => a) Wrodzone nietrzymanie barwnika spowodowane jest mutacją w genie MECP2 w locus Xq28, kodującym aktywator jądrowego czynnika transkrypcyjnego kappa B. U płci męskiej wada jest zazwyczaj letalna. Istotą choroby jest niezdolność komórek podstawnych skóry do gromadzenia melaniny, która gromadzi się w skórze właściwej oraz w makrofagach indukując stan zapalny.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1440
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1448] => Array
                                                        (
                                                            [id] => 1448
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 393
                                                            [name] => b) Zespół Retta spowodowany jest mutacją lub aberracją w genie IKBKG, locus Xq28. Jest to szereg zaburzeń neurorozwojowych, które w większości wypadków prowadzą do znacznej i głębokiej niepełnosprawności ruchowej oraz znacząco ograniczają możliwość komunikacji z otoczeniem.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1441
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1449] => Array
                                                        (
                                                            [id] => 1449
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 393
                                                            [name] => c) Zespół Aicardiego to zespół wrodzonych wad genetycznych charakteryzujący się częściowym lub całkowitym brakiem ciała modzelowatego, obecnością zmian w siatkówce i napadów drgawkowych.
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1442
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1450] => Array
                                                        (
                                                            [id] => 1450
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 393
                                                            [name] => d) Letalne dysplazje kostne u płodu, takie jak dysplazja tanatoforyczna oraz wrodzona łamliwości kości typu III odpowiedzialne są za przyczynę utraty ciąży.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1443
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [138] => Array
                                        (
                                            [id] => 138
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Termin sekwencjonowanie następnej generacji oznacza :
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [463] => Array
                                                        (
                                                            [id] => 463
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 138
                                                            [name] => a. Analizę całego genomu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 456
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [464] => Array
                                                        (
                                                            [id] => 464
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 138
                                                            [name] => b. Analizę całego eksomu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 457
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [465] => Array
                                                        (
                                                            [id] => 465
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 138
                                                            [name] => c. Sposób badania, ale nie jego zakres
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 458
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [466] => Array
                                                        (
                                                            [id] => 466
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 138
                                                            [name] => d. Analizę panelu genów
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 459
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [394] => Array
                                        (
                                            [id] => 394
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Oznaczenie płci płodu jest konieczne w przypadku diagnostyki prenatalnej:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1451] => Array
                                                        (
                                                            [id] => 1451
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 394
                                                            [name] => a) Mukowiscydozy
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1444
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1452] => Array
                                                        (
                                                            [id] => 1452
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 394
                                                            [name] => b) Zespołu duplikacji MECP2
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1445
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1453] => Array
                                                        (
                                                            [id] => 1453
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 394
                                                            [name] => c) Rdzeniowego zaniku mięśni
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1446
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1454] => Array
                                                        (
                                                            [id] => 1454
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 394
                                                            [name] => d) Zespołu Angelmana
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1447
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [139] => Array
                                        (
                                            [id] => 139
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 2
                                            [name] => Zaznacz zdanie fałszywe:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [467] => Array
                                                        (
                                                            [id] => 467
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 139
                                                            [name] => a. Pokrycie badanych regionów genu odnosi się do liczby odczytów tych fragmentów
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 460
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [468] => Array
                                                        (
                                                            [id] => 468
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 139
                                                            [name] => b. Każde laboratorium definiuje we własnym zakresie liczbę i rodzaj genów analizowanych w ramach danego panelu na podstawie baz danych i dostępnej literatury
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 461
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [469] => Array
                                                        (
                                                            [id] => 469
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 139
                                                            [name] => c. Ocena patogenności wariantów jest jednym z podstawowych wyzwań diagnostyki molekularnej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 462
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [470] => Array
                                                        (
                                                            [id] => 470
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 139
                                                            [name] => d. Sekwencjonowanie Sangera nie umożliwia identyfikacji nowych mutacji, nie opisanych wcześniej w piśmiennictwie
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 463
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [395] => Array
                                        (
                                            [id] => 395
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Do Poradni Genetycznej zgłosiła się 25-letnia kobieta z potwierdzonym molekularnie przedwczesnym wygasaniem czynności jajników związanym z FraX (premutacja w genie FMR1) w celu ewentualnej diagnostyki prenatalnej. Do przeprowadzenia badania wykorzystana zostanie technika:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1455] => Array
                                                        (
                                                            [id] => 1455
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 395
                                                            [name] => a) PCR z analizą GeneScan i/lub Triplet-Primed PCR (TP-PCR)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1448
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1456] => Array
                                                        (
                                                            [id] => 1456
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 395
                                                            [name] => b) Sekwencjonowanie następnej generacji celowane
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1449
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1457] => Array
                                                        (
                                                            [id] => 1457
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 395
                                                            [name] => c) Sekwencjonowanie techniką Sangera genu FMR1
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1450
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1458] => Array
                                                        (
                                                            [id] => 1458
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 395
                                                            [name] => d) Pacjentce nie powinno się wykonywać diagnostyki prenatalnej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1451
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [140] => Array
                                        (
                                            [id] => 140
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Stwierdzenie, że u danego pacjenta najprawdopodobniej wystąpiła mutacja de novo możliwe jest poprzez:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [471] => Array
                                                        (
                                                            [id] => 471
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 140
                                                            [name] => a. Zastosowanie sekwencjonowania NGS jako metody diagnostycznej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 464
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [472] => Array
                                                        (
                                                            [id] => 472
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 140
                                                            [name] => b. Analizę rodowodu i fakt, iż choroba nie występowała wcześniej u żadnego z krewnych Pacjenta bez konieczności wykonania analiz u rodziców pacjenta
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 465
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [473] => Array
                                                        (
                                                            [id] => 473
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 140
                                                            [name] => c. Wykonanie badania rodziców pacjenta i wykluczenie u obojga z nich obecności danej mutacji
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 466
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [396] => Array
                                        (
                                            [id] => 396
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Ryzyko otrzymania wyniku fałszywie pozytywnego dla trisomii w badaniu przesiewowym z wykorzystaniem wolnego płodowego DNA rośnie w przypadku:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1459] => Array
                                                        (
                                                            [id] => 1459
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 396
                                                            [name] => a) „vanishing twin”
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1452
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1460] => Array
                                                        (
                                                            [id] => 1460
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 396
                                                            [name] => b) Nieprawidłowości chromosomowych u matki
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1453
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1461] => Array
                                                        (
                                                            [id] => 1461
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 396
                                                            [name] => c) Mozaikowości
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1454
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1462] => Array
                                                        (
                                                            [id] => 1462
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 396
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1455
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [141] => Array
                                        (
                                            [id] => 141
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Określenie Kraniostenoza oznacza:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [474] => Array
                                                        (
                                                            [id] => 474
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 141
                                                            [name] => a. Ścieśnienie czaszki na skutek przedwczesnego zarastania szwów czaszkowych
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 467
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [475] => Array
                                                        (
                                                            [id] => 475
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 141
                                                            [name] => b. Zarośnięcie pojedynczego szwu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 468
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [476] => Array
                                                        (
                                                            [id] => 476
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 141
                                                            [name] => c. Zwężenie w strukturach wewnątrz czaszki
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 469
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [477] => Array
                                                        (
                                                            [id] => 477
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 141
                                                            [name] => d. Zwężenie dotyczące oczodołów
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 470
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [397] => Array
                                        (
                                            [id] => 397
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Ryzyko otrzymania wyniku fałszywie negatywnego dla trisomii w badaniu przesiewowym z wykorzystaniem wolnego płodowego DNA rośnie w przypadku:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1463] => Array
                                                        (
                                                            [id] => 1463
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 397
                                                            [name] => a) Aberracja obecna jedynie w komórkach płodu, brak w trofoblaście (TFM ang. true fetal mosaicism)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1456
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1464] => Array
                                                        (
                                                            [id] => 1464
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 397
                                                            [name] => b) Zbyt niski % frakcji płodowego DNA (>4%)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1457
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1465] => Array
                                                        (
                                                            [id] => 1465
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 397
                                                            [name] => c) Złe przechowywanie próbek z krwią pacjentek
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1458
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1466] => Array
                                                        (
                                                            [id] => 1466
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 397
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1459
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [142] => Array
                                        (
                                            [id] => 142
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Do genów, których patogenne mutacje uznawane są za przyczynę rozwoju przewlekłego zapalenia trzustki i  dziedziczą się autosomalnie dominująco zaliczamy: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [478] => Array
                                                        (
                                                            [id] => 478
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 142
                                                            [name] => a. gen PRSS1
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 471
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [479] => Array
                                                        (
                                                            [id] => 479
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 142
                                                            [name] => b. gen CFTR, SPINK1, CTRC
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 472
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [480] => Array
                                                        (
                                                            [id] => 480
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 142
                                                            [name] => c. gen CPA1
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 473
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [481] => Array
                                                        (
                                                            [id] => 481
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 142
                                                            [name] => d. odpowiedzi A i C są prawidłowe
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 474
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [398] => Array
                                        (
                                            [id] => 398
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Podczas badania całoeksomowego badamy:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1467] => Array
                                                        (
                                                            [id] => 1467
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 398
                                                            [name] => a) Wszystkie części kodujące genomu
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1460
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1468] => Array
                                                        (
                                                            [id] => 1468
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 398
                                                            [name] => b) Kilka lub kilkanaście wybranych genów
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1461
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1469] => Array
                                                        (
                                                            [id] => 1469
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 398
                                                            [name] => c) Części niekodujące genomu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1462
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1470] => Array
                                                        (
                                                            [id] => 1470
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 398
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1463
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [143] => Array
                                        (
                                            [id] => 143
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Według polskich i europejskich rekomendacji badania genetyczne u pacjentów z przewlekłym zapaleniem trzustki należy wykonać w przypadku: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [482] => Array
                                                        (
                                                            [id] => 482
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 143
                                                            [name] => a. alkoholowego  PZT
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 475
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [483] => Array
                                                        (
                                                            [id] => 483
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 143
                                                            [name] => b. u pacjentów z  pozytywnym wywiadem rodzinnym
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 476
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [484] => Array
                                                        (
                                                            [id] => 484
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 143
                                                            [name] => c. u pacjentów z  o wczesnym początku zachorowania lub/i  niejasnej etiologii
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 477
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [485] => Array
                                                        (
                                                            [id] => 485
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 143
                                                            [name] => d. odpowiedz B i C są prawidłowe
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 478
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [144] => Array
                                        (
                                            [id] => 144
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 18
                                            [type_id] => 1
                                            [name] => Wrodzone Wady Metabolizmu mogą dziedziczyć się :
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [486] => Array
                                                        (
                                                            [id] => 486
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                                                            [name] => a. Analiza genu DMPK pod kątem obecności delecji obejmujących jeden lub więcej eksonów z wykorzystaniem techniki MLPA
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 851
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [859] => Array
                                                        (
                                                            [id] => 859
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 238
                                                            [name] => b. Analiza genu DMPK pod kątem obecności ekspansji sekwencji CTG (>50 powtórzeń) z zastosowaniem techniki TP-PCR
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 852
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [860] => Array
                                                        (
                                                            [id] => 860
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 238
                                                            [name] => c. Analiza sekwencji kodującej genu DMPK w celu identyfikacji mutacji punktowych powodujących utratę funkcji białka
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 853
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [861] => Array
                                                        (
                                                            [id] => 861
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 238
                                                            [name] => d. Sekwencjonowanie następnej generacji obejmujące panel genów związanych z chorobami nerwowo-mięśniowymi
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 854
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [239] => Array
                                        (
                                            [id] => 239
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 19
                                            [type_id] => 1
                                            [name] => U dwojga dzieci 40 letniego zdrowego mężczyzny występują objawy tej samej choroby dziedziczonej autosomalnie dominująco. Ojciec mężczyzny również wykazuje objawy tej samej choroby co jego wnuki. U wszystkich osób zidentyfikowano obecność tej samej heterozygotycznej patogennej mutacji. Proszę podać, która z poniższych możliwości najlepiej definiuje zaistniałą sytuację?
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [862] => Array
                                                        (
                                                            [id] => 862
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 239
                                                            [name] => a. Zróżnicowany, wewnątrzrodzinny stopień ekspresji klinicznej choroby
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 855
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [863] => Array
                                                        (
                                                            [id] => 863
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 239
                                                            [name] => b. Heterogenność alleliczna
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 856
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [864] => Array
                                                        (
                                                            [id] => 864
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 239
                                                            [name] => c. Brak penetracji mutacji u 40 letniego mężczyzny, ojca chorych dzieci
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 857
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [865] => Array
                                                        (
                                                            [id] => 865
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 239
                                                            [name] => d. Mozaikowość germinalna
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 858
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [240] => Array
                                        (
                                            [id] => 240
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 19
                                            [type_id] => 1
                                            [name] => Wykonanie testów predykcyjnych u osoby 25-cio letniej, która ma bliskiego krewnego z chorobą Huntingtona (wskaż błędne stwierdzenie):
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [866] => Array
                                                        (
                                                            [id] => 866
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 240
                                                            [name] => a. umożliwia określenie ryzyka wystąpienia choroby w wieku późniejszym
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 859
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [867] => Array
                                                        (
                                                            [id] => 867
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 240
                                                            [name] => b. stwierdzenie mutacji oznacza, że objawy choroby mogą, ale nie muszą wystąpić w przyszłości
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 860
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [868] => Array
                                                        (
                                                            [id] => 868
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 240
                                                            [name] => c. stwierdzenie mutacji oznacza, że objawy choroby na pewno wystąpią, jest to kwestia czasu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 861
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [869] => Array
                                                        (
                                                            [id] => 869
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 240
                                                            [name] => d. powinno być poprzedzone poradą genetyczna oraz konsultacja psychologiczną
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 862
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [241] => Array
                                        (
                                            [id] => 241
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 19
                                            [type_id] => 1
                                            [name] => Które z badań nie ma zastosowania w diagnostyce chorób nerwów obwodowych:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [870] => Array
                                                        (
                                                            [id] => 870
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 241
                                                            [name] => a. EMG
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 863
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [871] => Array
                                                        (
                                                            [id] => 871
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 241
                                                            [name] => b. Badanie genetyczne
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 864
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [872] => Array
                                                        (
                                                            [id] => 872
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 241
                                                            [name] => c. Rezonans magnetyczny mózgu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 865
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [873] => Array
                                                        (
                                                            [id] => 873
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 241
                                                            [name] => d. EEG
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 866
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [242] => Array
                                        (
                                            [id] => 242
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 19
                                            [type_id] => 1
                                            [name] => Zespół łamliwego chromosomu X:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [874] => Array
                                                        (
                                                            [id] => 874
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 242
                                                            [name] => a. jest chorobą nie sprzężoną z płcią
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 867
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [875] => Array
                                                        (
                                                            [id] => 875
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 242
                                                            [name] => b. za chorobę odpowiada mutacja dynamiczna w genie FMR1
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 868
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [876] => Array
                                                        (
                                                            [id] => 876
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 242
                                                            [name] => c. za chorobę odpowiada premutacja w genie FMR1
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 869
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [877] => Array
                                                        (
                                                            [id] => 877
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 242
                                                            [name] => d. wszystkie odpowiedzi są prawidłowe
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 870
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [243] => Array
                                        (
                                            [id] => 243
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 19
                                            [type_id] => 1
                                            [name] => Neuropatia z nadwrażliwością na ucisk (HNPP) spowodowane jest:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [878] => Array
                                                        (
                                                            [id] => 878
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 243
                                                            [name] => a. Delecją w genie PMP22
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 871
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [879] => Array
                                                        (
                                                            [id] => 879
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 243
                                                            [name] => b. Duplikacją genu PMP22
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 872
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [880] => Array
                                                        (
                                                            [id] => 880
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 243
                                                            [name] => c. Może być obrazem przewlekłej neuropatii zapalnej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 873
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [881] => Array
                                                        (
                                                            [id] => 881
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 243
                                                            [name] => d. Mutacja genu LITA
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 874
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [244] => Array
                                        (
                                            [id] => 244
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 19
                                            [type_id] => 2
                                            [name] => Zaznacz zdanie nieprawdziwe:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [882] => Array
                                                        (
                                                            [id] => 882
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 244
                                                            [name] => a. Niepełnosprawność intelektualną definiuje się jako istotne obniżenie ogólnego funkcjonowania intelektualnego oraz deficyty w zakresie zachowań adaptacyjnych.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 875
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [883] => Array
                                                        (
                                                            [id] => 883
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 244
                                                            [name] => b. Uważa się, że około 50% przypadków niepełnosprawności intelektualnej w stopniu umiarkowanym i znacznym ma podłoże genetyczne.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 876
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [884] => Array
                                                        (
                                                            [id] => 884
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 244
                                                            [name] => c. Najczęstszą przyczyną niepełnosprawności intelektualnej są mutacje w pojedynczych genach
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 877
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [885] => Array
                                                        (
                                                            [id] => 885
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 244
                                                            [name] => d. Zastosowanie w diagnostyce niepełnosprawności intelektualnej wysokoprzepustowych metod analizy (m.in. NGS) pozwoliło na uzyskanie ponad 60% skuteczności diagnostycznej w tej grupie chorób.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 878
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [245] => Array
                                        (
                                            [id] => 245
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 19
                                            [type_id] => 1
                                            [name] => Chorobą nerwowo-mięśniową, w której stwierdza się zaburzenia działania połączeń nerwowo-mięśniowych jest:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [886] => Array
                                                        (
                                                            [id] => 886
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 245
                                                            [name] => a. Rdzeniowy zanik mięśni
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 879
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [887] => Array
                                                        (
                                                            [id] => 887
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 245
                                                            [name] => b. Zespół synaptyczny
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 880
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [888] => Array
                                                        (
                                                            [id] => 888
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 245
                                                            [name] => c. Dystrofia mięśniowa Beckera
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 881
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [889] => Array
                                                        (
                                                            [id] => 889
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 245
                                                            [name] => d. Dystrofia miotoniczna typu I
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 882
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [246] => Array
                                        (
                                            [id] => 246
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 19
                                            [type_id] => 1
                                            [name] => Sekwencjonowanie następnej generacji (NGS) stało się ostatnio metodą wykorzystywaną zarówno w diagnostyce jaki identyfikacji nowych genów stanowiących podłoże molekularne chorób genetycznych o dziedziczeniu mendlowskim. W przypadku ciężkich postaci niepełnosprawności intelektualnej i encefalopatii padaczkowych, występujących zazwyczaj sporadycznie. Przy założeniu, że mutacje patogenne mają charakter dominujący i występują de novo często stosuje się tzw. analizę triosów (pacjent + rodzice). Jakie warianty DNA należy brać tu pod uwagę przy rozpatrywaniu mutacji potencjalnie patogennych:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
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                                                )

                                        )

                                    [186] => Array
                                        (
                                            [id] => 186
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 20
                                            [type_id] => 2
                                            [name] => Wskaż zdanie błędne: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [657] => Array
                                                        (
                                                            [id] => 657
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 186
                                                            [name] => a. Sekwencjonowanie całego regionu kodującego nie umożliwia wykrycia 100% mutacji genu CFTR
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 650
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [658] => Array
                                                        (
                                                            [id] => 658
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 186
                                                            [name] => b.  W przesiewie noworodkowym: prawidłowe wyniki badania chlorków w pocie i wykrycie dwóch mutacji genu CFTR, z których najwyżej jedna jest zmianą o niejasnych konsekwencjach klinicznych umożliwia diagnozę mukowiscydozy mutacji genu CFTR, z których najwyżej jedna jest zmianą o niejasnych konsekwencjach klinicznych umożliwia diagnostykę mukowiscydozy
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 651
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [659] => Array
                                                        (
                                                            [id] => 659
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 186
                                                            [name] => c.  W Europie w przesiewie noworodkowym dzieci z granicznymi testami potowymi i bez wykrycia dwóch patogennych mutacji są zaliczane do CFSPID
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 652
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [660] => Array
                                                        (
                                                            [id] => 660
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 186
                                                            [name] => d.  Niektóre mutacje genu CFTR są związane zarówno z rozwojem chorób CFTR-zależnych, jak i mukowiscydozy, a u niektórych osób mogą nawet nie powodować żadnych objawów choroby.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 653
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [187] => Array
                                        (
                                            [id] => 187
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 20
                                            [type_id] => 1
                                            [name] => Choroby mitochondrialne mogą dziedziczyć się w sposób:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [661] => Array
                                                        (
                                                            [id] => 661
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 187
                                                            [name] => a. Wyłącznie odmatczyny
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 654
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [662] => Array
                                                        (
                                                            [id] => 662
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 187
                                                            [name] => b. Tylko autosomalny
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 655
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [663] => Array
                                                        (
                                                            [id] => 663
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 187
                                                            [name] => c. Tylko zgodnie z prawami Mendla
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 656
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [664] => Array
                                                        (
                                                            [id] => 664
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 187
                                                            [name] => d. W sposób odmatczyny lub zgodnie z prawami Mendla
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 657
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [188] => Array
                                        (
                                            [id] => 188
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 20
                                            [type_id] => 1
                                            [name] => Do analizy patogennych wariantów mitochondrialnego DNA najlepiej nadaje się DNA izolowany z:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [665] => Array
                                                        (
                                                            [id] => 665
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 188
                                                            [name] => a. Leukocytów krwi obwodowej, bo zwykle patogenne warianty mitochondrialnego DNA występują w nim na wysokim poziomie
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 658
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [666] => Array
                                                        (
                                                            [id] => 666
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 188
                                                            [name] => b. Erytrocytów, bo nie zawierają jąder komórkowych, więc uzyskuje się czysty mitochondrialny DNA do analizy.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 659
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [667] => Array
                                                        (
                                                            [id] => 667
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 188
                                                            [name] => c. Bioptatu mięśnia,  bo zwykle patogenne warianty mitochondrialnego DNA występują w nim na wysokim poziomie
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 660
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [668] => Array
                                                        (
                                                            [id] => 668
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 188
                                                            [name] => d. Hodowli fibroblastów, bo podczas hodowli następuje amplifikacja wariantu patogennego i łatwiej można go wykryć.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 661
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [189] => Array
                                        (
                                            [id] => 189
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 20
                                            [type_id] => 1
                                            [name] => Choroba Huntingtona (HD) to neurodegeneracyjna choroba o dziedziczeniu autosomalnym dominującym i późnym wieku zachorowania. W dziedziczeniu tej choroby występuje zjawisko antycypacji odojcowskiej. Jakie jest ryzyko zachorowania na HD córki mężczyzny, u którego objawy rozwinęły się w 45 roku życia?
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [669] => Array
                                                        (
                                                            [id] => 669
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 189
                                                            [name] => a. nie da się określić
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 662
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [670] => Array
                                                        (
                                                            [id] => 670
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 189
                                                            [name] => b. 50%
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 663
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [671] => Array
                                                        (
                                                            [id] => 671
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 189
                                                            [name] => c. 25%
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 664
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [672] => Array
                                                        (
                                                            [id] => 672
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 189
                                                            [name] => d. nie ma takiego ryzyka
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 665
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [190] => Array
                                        (
                                            [id] => 190
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 20
                                            [type_id] => 1
                                            [name] => Choroba Huntingtona (HD) to neurodegeneracyjna choroba o dziedziczeniu autosomalnym dominującym i późnym wieku zachorowania. W dziedziczeniu tej choroby występuje zjawisko antycypacji odojcowskiej. Występowanie antycypacji odojcowskiej w dziedziczeniu HD oznacza, że:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [673] => Array
                                                        (
                                                            [id] => 673
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 190
                                                            [name] => a. patogenny wariant genu zostaje wyciszony, ulega piętnowniu genomowemu, na chromosomie
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 666
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [674] => Array
                                                        (
                                                            [id] => 674
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 190
                                                            [name] => b. postać młodzieńcza choroby występuje tylko w dziedziczeniu choroby od ojca
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 667
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [675] => Array
                                                        (
                                                            [id] => 675
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 190
                                                            [name] => c. najcięższa postać choroby występuje w dziedziczeniu mutacji od matki w wyniku silnego
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 668
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [676] => Array
                                                        (
                                                            [id] => 676
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 190
                                                            [name] => d.  postać młodzieńcza/dziecięca choroby występuje głównie w dziedziczeniu choroby od ojca w wyniku silnego zwielokrotnienia liczby powtórzeń
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 669
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [191] => Array
                                        (
                                            [id] => 191
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 20
                                            [type_id] => 1
                                            [name] => Choroba Parkinsona o wczesnym początku zachorowania (<45 r.ż.), ma podłoże genetyczne, powodowana może być mutacjami w genach PARK2, PINK1 i DJ1. Najczęściej u pacjentów z rodzinną, wczesną postacią tej choroby identyfikowane są mutacje w genie PARK2 (około 40%).Wszystkie postaci dziedziczą się jako cecha autosomalna recesywna .Czy biorąc pod uwagę przedstawiony rodowód (wszyscy chorzy mają wczesną postać choroby Parkinsona), należy rozważyć przeprowadzenie testów genetycznych dla tych genów?
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [677] => Array
                                                        (
                                                            [id] => 677
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 191
                                                            [name] => a.  tak – może to być forma autosomalna recesywna choroby Parkinsona
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 670
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [678] => Array
                                                        (
                                                            [id] => 678
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 191
                                                            [name] => b.  nie – cechy recesywne nie mogą „przeskakiwać” pokoleń
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 671
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [679] => Array
                                                        (
                                                            [id] => 679
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 191
                                                            [name] => c.  trudno powiedzieć
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 672
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [192] => Array
                                        (
                                            [id] => 192
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 20
                                            [type_id] => 1
                                            [name] => Wskaż prawidłową odpowiedź: Zespół łamliwego chromosomu X:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [680] => Array
                                                        (
                                                            [id] => 680
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 192
                                                            [name] => a. jest chorobą sprzężoną z chromosomem X
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 673
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [681] => Array
                                                        (
                                                            [id] => 681
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 192
                                                            [name] => b. jest najczęstszą przyczyną genetycznie uwarunkowanej niepełnosprawności intelektualnej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 674
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [682] => Array
                                                        (
                                                            [id] => 682
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 192
                                                            [name] => c. jest przykładem choroby epigenetycznej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 675
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [683] => Array
                                                        (
                                                            [id] => 683
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 192
                                                            [name] => d. wszystkie odpowiedzi są prawidłowe
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 676
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [684] => Array
                                                        (
                                                            [id] => 684
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 192
                                                            [name] => d. wszystkie odpowiedzi są prawidłowe
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 677
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [685] => Array
                                                        (
                                                            [id] => 685
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 192
                                                            [name] => e. prawidłowa jest odpowiedź A i C
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 678
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [193] => Array
                                        (
                                            [id] => 193
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 20
                                            [type_id] => 1
                                            [name] => Chłopiec z izolowaną formą niepełnosprawności intelektualnej w pierwszej kolejności powinien mieć wykonane badanie/a diagnostyczne: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [686] => Array
                                                        (
                                                            [id] => 686
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 193
                                                            [name] => a.        aCHG
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 679
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [687] => Array
                                                        (
                                                            [id] => 687
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 193
                                                            [name] => b.        aCGH, NGS
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 680
                                                            [correct_yesno] => Nie
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                                                            [question_id] => 358
                                                            [name] => b) we krwi obwodowej jest niemożliwe u pacjentów po przeszczepie szpiku
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1300
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1308] => Array
                                                        (
                                                            [id] => 1308
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 358
                                                            [name] => c) można wykonać we krwi, fibroblastach skóry, komórkach nabłonka policzka
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1301
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1309] => Array
                                                        (
                                                            [id] => 1309
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 358
                                                            [name] => d) nie wymaga pobrania krwi na czczo
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1302
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [359] => Array
                                        (
                                            [id] => 359
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 21
                                            [type_id] => 2
                                            [name] => Wrodzone wady serca:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [1310] => Array
                                                        (
                                                            [id] => 1310
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 359
                                                            [name] => a) zawsze występują jako cecha izolowana, a ich przyczyną są mutacje genów kodujących białka związane z rozwojem serca
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1303
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1311] => Array
                                                        (
                                                            [id] => 1311
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 359
                                                            [name] => b) mogą być spowodowane mutacjami w genach kodujących wyłącznie białka tworzące strukturę mięśnia sercowego
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1304
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1312] => Array
                                                        (
                                                            [id] => 1312
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 359
                                                            [name] => c) mogą występować zarówno jako cecha izolowana lub wada, której towarzyszą dodatkowe objawy kliniczne (tzw. wady syndromiczne)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1305
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1313] => Array
                                                        (
                                                            [id] => 1313
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 359
                                                            [name] => d) występują wyłącznie jako efekt mutacji w określonych genach lub aberracji chromosomowych o charakterze liczbowym
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1306
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [360] => Array
                                        (
                                            [id] => 360
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 21
                                            [type_id] => 2
                                            [name] => Choroby z grupy RASopatii to:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [1314] => Array
                                                        (
                                                            [id] => 1314
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 360
                                                            [name] => a) zespoły wad wrodzonych, którym zawsze towarzyszy wada serca np. zwężenie zastawki tętnicy płucnej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1307
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1315] => Array
                                                        (
                                                            [id] => 1315
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 360
                                                            [name] => b) grupa heterogennych klinicznie chorób, w których przebiegu może wystąpić izolowana wada serca
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1308
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1316] => Array
                                                        (
                                                            [id] => 1316
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 360
                                                            [name] => c) grupa chorób o wysokiej heterogenności genetycznej, wykazujących zmienną ekspresję objawów klinicznych
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1309
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1317] => Array
                                                        (
                                                            [id] => 1317
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 360
                                                            [name] => d) zespoły wad wrodzonych, w których wadzie serca towarzyszą zmiany skórne i przykurcze mięśni kończyn dolnych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1310
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [361] => Array
                                        (
                                            [id] => 361
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 21
                                            [type_id] => 1
                                            [name] => Najbardziej efektywną techniką, którą stosuje się w diagnostyce monogenowych zespołów wad wrodzonych, o wysokiej heterogenności genetycznej i klinicznej, w przebiegu których występują wrodzone wady serca, jest:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1318] => Array
                                                        (
                                                            [id] => 1318
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 361
                                                            [name] => a) sekwencjonowanie następnej generacji
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1311
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1319] => Array
                                                        (
                                                            [id] => 1319
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 361
                                                            [name] => b) sekwencjonowanie metodą Sangera
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1312
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1320] => Array
                                                        (
                                                            [id] => 1320
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 361
                                                            [name] => c) ilościowy PCR w czasie rzeczywistym
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1313
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1321] => Array
                                                        (
                                                            [id] => 1321
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 361
                                                            [name] => d) analiza kariotypu z badaniem FISH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1314
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [399] => Array
                                        (
                                            [id] => 399
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 21
                                            [type_id] => 1
                                            [name] => Ryzyko aberracji chromosomowej u płodu nie będzie zwiększone w przypadku rozpoznania w badaniu ECHO serca płodu następującej wady serca:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1471] => Array
                                                        (
                                                            [id] => 1471
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 399
                                                            [name] => a) Całkowity kanał przedsionkowo-komorowy (AVSD)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1464
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1472] => Array
                                                        (
                                                            [id] => 1472
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 399
                                                            [name] => b) Duży ubytek przegrody międzykomorowej w części napływowej (VSD)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1465
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1473] => Array
                                                        (
                                                            [id] => 1473
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 399
                                                            [name] => c) Podwójne odejście naczyń z prawej komory (DORV)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1466
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1474] => Array
                                                        (
                                                            [id] => 1474
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 399
                                                            [name] => d) Zespół Fallota (TOF)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1467
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1475] => Array
                                                        (
                                                            [id] => 1475
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 399
                                                            [name] => e) Proste przełożenie wielkich pni tętniczych (TGA)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1468
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [400] => Array
                                        (
                                            [id] => 400
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 21
                                            [type_id] => 1
                                            [name] => W przypadku rozpoznania wady serca u płodu istnieje możliwość wykonania dodatkowych badań diagnostycznych. Wskaż prawidłową odpowiedź:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1476] => Array
                                                        (
                                                            [id] => 1476
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 400
                                                            [name] => a) wystarczającym badaniem jest klasyczny kariotyp
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1469
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1477] => Array
                                                        (
                                                            [id] => 1477
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 400
                                                            [name] => b) w większości przypadków zalecane jest badanie metodą aCGH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1470
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1478] => Array
                                                        (
                                                            [id] => 1478
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 400
                                                            [name] => c) w niektórych przypadkach istnieje możliwość badania określonych zespołów monogenowych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1471
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1479] => Array
                                                        (
                                                            [id] => 1479
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 400
                                                            [name] => d) w przypadku rozpoznania wady serca u płodu nie ma wskazań do badań inwazyjnych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1472
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1480] => Array
                                                        (
                                                            [id] => 1480
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 400
                                                            [name] => e) prawidłowe są odpowiedzi B i C
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1473
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [401] => Array
                                        (
                                            [id] => 401
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 21
                                            [type_id] => 1
                                            [name] => Przykładem aberracji chromosomowej , w której często występuje wada serca jest:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1481] => Array
                                                        (
                                                            [id] => 1481
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 401
                                                            [name] => a) Zespół Downa
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1474
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1482] => Array
                                                        (
                                                            [id] => 1482
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 401
                                                            [name] => b) Zespół Edwardsa
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1475
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1483] => Array
                                                        (
                                                            [id] => 1483
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 401
                                                            [name] => c) Zespół Turnera
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1476
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1484] => Array
                                                        (
                                                            [id] => 1484
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 401
                                                            [name] => d) Wszystkie wymienione zespoły
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1477
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [402] => Array
                                        (
                                            [id] => 402
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 21
                                            [type_id] => 1
                                            [name] => Jaki typ uwarunkowania genetycznego spotykamy w zespołach monogenowych z chorobami układu sercowo-naczyniowego:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1485] => Array
                                                        (
                                                            [id] => 1485
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 402
                                                            [name] => a) Autosomalny dominujący
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1478
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1486] => Array
                                                        (
                                                            [id] => 1486
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 402
                                                            [name] => b) Autosomalny recesywny
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1479
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1487] => Array
                                                        (
                                                            [id] => 1487
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 402
                                                            [name] => c) Sprzężony z chromosomem X
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1480
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [1488] => Array
                                                        (
                                                            [id] => 1488
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 402
                                                            [name] => d) Wszystkie wymienione
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1481
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [403] => Array
                                        (
                                            [id] => 403
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 21
                                            [type_id] => 1
                                            [name] => Wskaż BŁĘDNĄ odpowiedź:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [1489] => Array
                                                        (
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                                                            [status_code] => active
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                                            [name] => Zaznacz zdanie nieprawdziwe:
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                                                            [name] => a. Objawy zespołu dziecka wiotkiego mogą wystąpić jako konsekwencja powikłań w trakcie ciąży i porodu takich jak wcześniactwo, niedotlenienie
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                                                            [correct_yesno] => Nie
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                                                            [id] => 1061
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                                                            [question_id] => 288
                                                            [name] => b. Mianem zespołu dziecka wiotkiego określa się wyłącznie grupę jednostek chorobowych związanych z zaburzeniami funkcjonowania układu nerwowo-mięśniowego
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                                                            [ext] => 
                                                            [sort] => 1054
                                                            [correct_yesno] => Tak
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                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                            [ext] => 
                                                            [sort] => 1055
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
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                                                            [id] => 1063
                                                            [site_id] => 1
                                                            [status_id] => 5
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                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1056
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
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                                            [name] => Sekwencjonowanie następnej generacji (NGS) stało się ostatnio metodą wykorzystywaną zarówno w diagnostyce jaki identyfikacji nowych genów stanowiących podłoże molekularne chorób genetycznych o dziedziczeniu mendlowskim. W przypadku ciężkich postaci niepełnosprawności intelektualnej i encefalopatii padaczkowych, występujących zazwyczaj sporadycznie, przy założeniu, że mutacje patogenne mają charakter dominujący i występują de novo często stosuje się tzw. analizę triosów.Metoda ta polega na równoczesnej analizie wariantów występujących u rodziców i chorego dziecka.Jakie warianty należy brać pod uwagę jako patogenne:
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                                                            [name] => b. warianty heterozygotyczne (występujące w jednym allelu genu), które nie występują u żadnego z
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                                                            [ext] => 
                                                            [sort] => 1058
                                                            [correct_yesno] => Tak
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                                                            [id] => 1066
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                                                            [question_id] => 289
                                                            [name] => c. warianty identyfikowane w dwóch allelach genu (homozygotyczne, heterozygotyczne złożone)
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                                                            [ext] => 
                                                            [sort] => 1059
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                            [question_id] => 289
                                                            [name] => d. warianty homozygotyczne, z których jeden został odziedziczony po rodzicu.
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                                                            [status_code] => active
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                                            [name] => Chorobę genetyczną u noworodka można podejrzewać w następujących przypadkach z wyjątkiem:
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                                                            [name] => b. u dziecka spokrewnionych rodziców stwierdzono objawy kwasicy metabolicznej
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                                                            [ext] => 
                                                            [sort] => 1063
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                                                            [status_name] => Aktywny
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                                                            [name] => d. matka w czasie ciąży była narażona na działanie silnego czynnika teratogennego (alkohol)
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                                                            [ext] => 
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                                                            [correct_yesno] => Tak
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                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                            [name] => Badanie chromosomów metodą kariotyp HRT umożliwia identyfikację aberracji większych niż
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                                            [sort] => 0
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                                                            [sort] => 1065
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                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 1066
                                                            [correct_yesno] => Tak
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                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                            [name] => c. 50 tysięcy par zasad
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                                                            [correct_yesno] => Nie
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                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                            [question_id] => 291
                                                            [name] => d. 50 milionów par zasad
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                                                            [ext] => 
                                                            [sort] => 1068
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                            [status_id] => 5
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                                            [type_id] => 1
                                            [name] => Ryzyko genetyczne dla krewnych noworodka z izolowaną wadą cewy nerwowej (przepuklina oponowa odc. lędźwiowo-krzyżowego kręgosłupa) zależy od:
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                                            [sort] => 0
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                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
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                                                            [id] => 1076
                                                            [site_id] => 1
                                                            [status_id] => 5
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                                                            [name] => a. predyspozycji genetycznej (podatności) do wystąpienia tej wady w rodzinie
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                                                            [ext] => 
                                                            [sort] => 1069
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                        (
                                                            [id] => 1077
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 292
                                                            [name] => b. stopnia pokrewieństwa w stosunku do noworodka
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 1070
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                    [1078] => Array
                                                        (
                                                            [id] => 1078
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 292
                                                            [name] => c. częstości występowania tej wady w populacji
                                                            [correct] => 0
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                                                            [id] => 937
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 257
                                                            [name] => b) Rapid FISH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 930
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [938] => Array
                                                        (
                                                            [id] => 938
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 257
                                                            [name] => c) MLPA
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 931
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [939] => Array
                                                        (
                                                            [id] => 939
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 257
                                                            [name] => d) Kariotyp
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 932
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [258] => Array
                                        (
                                            [id] => 258
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Zaznacz BŁĘDNE zdanie:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [940] => Array
                                                        (
                                                            [id] => 940
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 258
                                                            [name] => a) Wszystkie kobiety ciężarne powinny mieć zaproponowane przesiewowe badania prenatalne
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 933
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [941] => Array
                                                        (
                                                            [id] => 941
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 258
                                                            [name] => b) Badania inwazyjne powinny być wykonane po uprzednich badaniach przesiewowych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 934
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [942] => Array
                                                        (
                                                            [id] => 942
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 258
                                                            [name] => c) Badania przesiewowe nie określają ryzyka wystąpienia aberracji chromosomowych
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 935
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [943] => Array
                                                        (
                                                            [id] => 943
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 258
                                                            [name] => d) Kobietom, które decydują się na pominięcie etapu skriningowego, należy umożliwić wykonanie badania inwazyjnego po uprzednim poinformowaniu o możliwych powikłaniach
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 936
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [259] => Array
                                        (
                                            [id] => 259
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 2
                                            [name] => Które czynniki genetyczne należą do najczęstszych przyczyn niepowodzeń ciąży?
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [944] => Array
                                                        (
                                                            [id] => 944
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 259
                                                            [name] => a) choroby jednogenowe zarodka/płodu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 937
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [945] => Array
                                                        (
                                                            [id] => 945
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 259
                                                            [name] => b) disomia jednorodzicielska
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 938
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [946] => Array
                                                        (
                                                            [id] => 946
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 259
                                                            [name] => c) aberracje chromosomowe
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 939
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [947] => Array
                                                        (
                                                            [id] => 947
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 259
                                                            [name] => d) polimorfizmy i mutacje w genach, związane z różnymi procesami zachodzącymi w komórkach, takimi jak na przykład: immunosupresja, apoptoza, angiogeneza, czy przekazywanie sygnałów w komórce.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 940
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [260] => Array
                                        (
                                            [id] => 260
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Zaznacz PRAWIDŁOWE zdanie:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [948] => Array
                                                        (
                                                            [id] => 948
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 260
                                                            [name] => a) Wrodzone nietrzymanie barwnika spowodowane jest mutacją w genie MECP2 w locus Xq28, kodującym aktywator jądrowego czynnika transkrypcyjnego kappa B. U płci męskiej wada jest zazwyczaj letalna. Istotą choroby jest niezdolność komórek podstawnych skóry do gromadzenia melaniny, która gromadzi się w skórze właściwej oraz w makrofagach indukując stan zapalny.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 941
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [949] => Array
                                                        (
                                                            [id] => 949
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 260
                                                            [name] => b) Zespół Retta spowodowany jest mutacją lub aberracją w genie IKBKG, locus Xq28. Jest to szereg zaburzeń neurorozwojowych, które w większości wypadków prowadzą do znacznej i głębokiej niepełnosprawności ruchowej oraz znacząco ograniczają możliwość komunikacji z otoczeniem.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 942
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [950] => Array
                                                        (
                                                            [id] => 950
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 260
                                                            [name] => c) Zespół Aicardiego to zespół wrodzonych wad genetycznych charakteryzujący się częściowym lub całkowitym brakiem ciała modzelowatego, obecnością zmian w siatkówce i napadów drgawkowych.
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 943
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [951] => Array
                                                        (
                                                            [id] => 951
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 260
                                                            [name] => d) Letalne dysplazje kostne u płodu, takie jak dysplazja tanatoforyczna oraz wrodzona łamliwości kości typu III odpowiedzialne są za przyczynę utraty ciąży.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 944
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [261] => Array
                                        (
                                            [id] => 261
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Oznaczenie płci płodu jest konieczne w przypadku diagnostyki prenatalnej:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [952] => Array
                                                        (
                                                            [id] => 952
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 261
                                                            [name] => a) Mukowiscydozy
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 945
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [953] => Array
                                                        (
                                                            [id] => 953
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 261
                                                            [name] => b) Zespołu duplikacji MECP2
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 946
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [954] => Array
                                                        (
                                                            [id] => 954
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 261
                                                            [name] => c) Rdzeniowego zaniku mięśni
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 947
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [955] => Array
                                                        (
                                                            [id] => 955
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 261
                                                            [name] => d) Zespołu Angelmana
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 948
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [262] => Array
                                        (
                                            [id] => 262
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Do Poradni Genetycznej zgłosiła się 25-letnia kobieta z potwierdzonym molekularnie przedwczesnym wygasaniem czynności jajników związanym z FraX (premutacja w genie FMR1) w celu ewentualnej diagnostyki prenatalnej. Do przeprowadzenia badania wykorzystana zostanie technika:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [956] => Array
                                                        (
                                                            [id] => 956
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 262
                                                            [name] => a) PCR z analizą GeneScan i/lub Triplet-Primed PCR (TP-PCR)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 949
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [957] => Array
                                                        (
                                                            [id] => 957
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 262
                                                            [name] => b) Sekwencjonowanie następnej generacji celowane
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 950
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [958] => Array
                                                        (
                                                            [id] => 958
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 262
                                                            [name] => c) Sekwencjonowanie techniką Sangera genu FMR1
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 951
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [959] => Array
                                                        (
                                                            [id] => 959
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 262
                                                            [name] => d) Pacjentce nie powinno się wykonywać diagnostyki prenatalnej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 952
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [263] => Array
                                        (
                                            [id] => 263
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Ryzyko otrzymania wyniku fałszywie pozytywnego dla trisomii w badaniu przesiewowym z wykorzystaniem wolnego płodowego DNA rośnie w przypadku:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [960] => Array
                                                        (
                                                            [id] => 960
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 263
                                                            [name] => a) „vanishing twin”
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 953
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [961] => Array
                                                        (
                                                            [id] => 961
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 263
                                                            [name] => b) Nieprawidłowości chromosomowych u matki
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 954
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [962] => Array
                                                        (
                                                            [id] => 962
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 263
                                                            [name] => c) Mozaikowości
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 955
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [963] => Array
                                                        (
                                                            [id] => 963
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 263
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 956
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [264] => Array
                                        (
                                            [id] => 264
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Ryzyko otrzymania wyniku fałszywie negatywnego dla trisomii w badaniu przesiewowym z wykorzystaniem wolnego płodowego DNA rośnie w przypadku:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [964] => Array
                                                        (
                                                            [id] => 964
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 264
                                                            [name] => a) Aberracja obecna jedynie w komórkach płodu, brak w trofoblaście (TFM ang. true fetal mosaicism)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 957
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [965] => Array
                                                        (
                                                            [id] => 965
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 264
                                                            [name] => b) Zbyt niski % frakcji płodowego DNA (>4%)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 958
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [966] => Array
                                                        (
                                                            [id] => 966
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 264
                                                            [name] => c) Złe przechowywanie próbek z krwią pacjentek
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 959
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [967] => Array
                                                        (
                                                            [id] => 967
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 264
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 960
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [265] => Array
                                        (
                                            [id] => 265
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Podczas badania całoeksomowego badamy:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [968] => Array
                                                        (
                                                            [id] => 968
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 265
                                                            [name] => a) Wszystkie części kodujące genomu
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 961
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [969] => Array
                                                        (
                                                            [id] => 969
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 265
                                                            [name] => b) Kilka lub kilkanaście wybranych genów
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 962
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [970] => Array
                                                        (
                                                            [id] => 970
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 265
                                                            [name] => c) Części niekodujące genomu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 963
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [971] => Array
                                                        (
                                                            [id] => 971
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 265
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 964
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [220] => Array
                                        (
                                            [id] => 220
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => W dziedziczeniu autosomalnym recesywnym: 1. Rodzice najczęściej są nosicielami mutacji w genie związanym z chorobą dziecka. 2. Rodzice nosiciele ponoszą ryzyko wynoszące 25% wystąpienia choroby u kolejnego potomstwa. 3. Nosiciel mutacji w jednym allelu genu jest osobą zdrową. 4. Osoba z chorobą o uwarunkowaniu autosomalnym recesywnym ma szanse na zdrowe potomstwo, jeśli u partnera zostanie wykluczone nosicielstwo mutacji w genie związanym z chorobą. 5. Pokrewieństwo zwiększa ryzyko wystąpienia choroby o tym uwarunkowaniu genetycznym. Odpowiedź prawidłowa to: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [790] => Array
                                                        (
                                                            [id] => 790
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 220
                                                            [name] => Tylko 2
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 783
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [791] => Array
                                                        (
                                                            [id] => 791
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 220
                                                            [name] => 1, 2, 3
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 784
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [792] => Array
                                                        (
                                                            [id] => 792
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 220
                                                            [name] => 2, 3, 5
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 785
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [793] => Array
                                                        (
                                                            [id] => 793
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 220
                                                            [name] => Wszystkie odpowiedzi są prawdziwe
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 786
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [221] => Array
                                        (
                                            [id] => 221
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Wskaż nieprawidłową odpowiedź: Weryfikacja obecności mikrodelecji regionu AZF chromosomu Y umożliwia m.in. 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [794] => Array
                                                        (
                                                            [id] => 794
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 221
                                                            [name] => a) Ustalenie przyczyny niepłodności
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 787
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [795] => Array
                                                        (
                                                            [id] => 795
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 221
                                                            [name] => b) Zaplanowanie dalszego postępowania z parą
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 788
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [796] => Array
                                                        (
                                                            [id] => 796
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 221
                                                            [name] => c) Ocenę szansy sukcesu w TESE, ART
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 789
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [797] => Array
                                                        (
                                                            [id] => 797
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 221
                                                            [name] => d) Ocenę ryzyka przekazania niepłodności potomstwu płci żeńskiej
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 790
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [222] => Array
                                        (
                                            [id] => 222
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Wskaż zdanie prawdziwe: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [798] => Array
                                                        (
                                                            [id] => 798
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 222
                                                            [name] => a) CBAVD jest wynikiem mutacji tylko w genie CFTR
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 791
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [799] => Array
                                                        (
                                                            [id] => 799
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 222
                                                            [name] => b) Premutacje genu FMR1 są przyczyną przedwczesnego wygasania funkcji jajników
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 792
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [800] => Array
                                                        (
                                                            [id] => 800
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 222
                                                            [name] => c) Jednym ze wskazań do badania genu CFTR jest występowanie CBAVD z towarzyszącą agenezją nerki
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 793
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [801] => Array
                                                        (
                                                            [id] => 801
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 222
                                                            [name] => d) Prawidłowy wynik kariotypu, analizy regionu AZF chromosomu Y i genu CFTR oznacza, że przyczyną oligozoospermii u Pacjenta nie jest czynnik genetyczny.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 794
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [223] => Array
                                        (
                                            [id] => 223
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Zaznacz odpowiedź prawidłową dotyczącą techniki MLPA wykorzystywanej w szybkiej diagnostyce aneuploidii u płodu:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [802] => Array
                                                        (
                                                            [id] => 802
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 223
                                                            [name] => a) wykrywa aberracje zrównoważone, nie wykrywa kontaminacji krwią matczyną
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 795
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [803] => Array
                                                        (
                                                            [id] => 803
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 223
                                                            [name] => b) nie wykrywa kontaminacji krwią matczyną, nie wykrywa mozaikowości, nie wykrywa triploidii
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 796
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [804] => Array
                                                        (
                                                            [id] => 804
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 223
                                                            [name] => c) wykrywa aberracje zrównoważone, wykrywa triploidię
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 797
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [805] => Array
                                                        (
                                                            [id] => 805
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 223
                                                            [name] => d) wykrywa triploidię, nie wykrywa aberracji zrównoważonych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 798
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [224] => Array
                                        (
                                            [id] => 224
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 2
                                            [name] => Które zdania NIE dotyczą zespołu Klinefeltera:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [806] => Array
                                                        (
                                                            [id] => 806
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 224
                                                            [name] => a) jest najczęstszą genetyczną przyczyną niepłodności męskiej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 799
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [807] => Array
                                                        (
                                                            [id] => 807
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 224
                                                            [name] => b) związany jest z azoospermią lub znaczną oligozoospermią
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 800
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [808] => Array
                                                        (
                                                            [id] => 808
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 224
                                                            [name] => c) zazwyczaj stwierdza się kariotyp mozaikowy
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 801
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [809] => Array
                                                        (
                                                            [id] => 809
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 224
                                                            [name] => d) występuje z częstością 1 na 500 mężczyzn
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 802
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [225] => Array
                                        (
                                            [id] => 225
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Zaznacz BŁĘDNE zdanie dotyczące chromosomów markerowych stwierdzanych u osób z niepłodnością 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [810] => Array
                                                        (
                                                            [id] => 810
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 225
                                                            [name] => a) Najczęściej stwierdza się markery pochodzące z chromosomów akrocentrycznych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 803
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [811] => Array
                                                        (
                                                            [id] => 811
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 225
                                                            [name] => b) Chromosomy markerowe wpływają na niepowodzenia rozrodu nosicieli, ponieważ zawierają geny związane z niepłodnością
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 804
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [812] => Array
                                                        (
                                                            [id] => 812
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 225
                                                            [name] => c) U osób niepłodnych najczęściej stwierdza się markery pochodzące z chromosomu 15.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 805
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [813] => Array
                                                        (
                                                            [id] => 813
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 225
                                                            [name] => d) Obecność chromosomu markerowego zaburza proces gametogenezy
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 806
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [226] => Array
                                        (
                                            [id] => 226
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Aby ustalić typ trisomii (prosta czy translokacyjna) należy wykonać badanie: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [814] => Array
                                                        (
                                                            [id] => 814
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 226
                                                            [name] => a) QF-PCR
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 807
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [815] => Array
                                                        (
                                                            [id] => 815
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 226
                                                            [name] => b) Rapid FISH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 808
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [816] => Array
                                                        (
                                                            [id] => 816
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 226
                                                            [name] => c) MLPA
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 809
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [817] => Array
                                                        (
                                                            [id] => 817
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 226
                                                            [name] => d) Kariotyp
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 810
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [227] => Array
                                        (
                                            [id] => 227
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Zaznacz BŁĘDNE zdanie:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [818] => Array
                                                        (
                                                            [id] => 818
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 227
                                                            [name] => a) Wszystkie kobiety ciężarne powinny mieć zaproponowane przesiewowe badania prenatalne
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 811
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [819] => Array
                                                        (
                                                            [id] => 819
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 227
                                                            [name] => b) Badania inwazyjne powinny być wykonane po uprzednich badaniach przesiewowych
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 812
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [820] => Array
                                                        (
                                                            [id] => 820
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 227
                                                            [name] => c) Badania przesiewowe nie określają ryzyka wystąpienia aberracji chromosomowych
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 813
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [821] => Array
                                                        (
                                                            [id] => 821
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 227
                                                            [name] => d) Kobietom, które decydują się na pominięcie etapu skriningowego, należy umożliwić wykonanie badania inwazyjnego po uprzednim poinformowaniu o możliwych powikłaniach
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 814
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [228] => Array
                                        (
                                            [id] => 228
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 2
                                            [name] => Które czynniki genetyczne należą do najczęstszych przyczyn niepowodzeń ciąży?
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [822] => Array
                                                        (
                                                            [id] => 822
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 228
                                                            [name] => a) choroby jednogenowe zarodka/płodu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 815
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [823] => Array
                                                        (
                                                            [id] => 823
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 228
                                                            [name] => b) disomia jednorodzicielska
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 816
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [824] => Array
                                                        (
                                                            [id] => 824
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 228
                                                            [name] => c) aberracje chromosomowe
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 817
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [825] => Array
                                                        (
                                                            [id] => 825
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 228
                                                            [name] => d) polimorfizmy i mutacje w genach, związane z różnymi procesami zachodzącymi w komórkach, takimi jak na przykład: immunosupresja, apoptoza, angiogeneza, czy przekazywanie sygnałów w komórce.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 818
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [229] => Array
                                        (
                                            [id] => 229
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Zaznacz prawidłowe zdanie:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [826] => Array
                                                        (
                                                            [id] => 826
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 229
                                                            [name] => a) Wrodzone nietrzymanie barwnika spowodowane jest mutacją w genie MECP2 w locus Xq28, kodującym aktywator jądrowego czynnika transkrypcyjnego kappa B. U płci męskiej wada jest zazwyczaj letalna. Istotą choroby jest niezdolność komórek podstawnych skóry do gromadzenia melaniny, która gromadzi się w skórze właściwej oraz w makrofagach indukując stan zapalny.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 819
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [827] => Array
                                                        (
                                                            [id] => 827
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 229
                                                            [name] => b) Zespół Retta spowodowany jest mutacją lub aberracją w genie IKBKG, locus Xq28. Jest to szereg zaburzeń neurorozwojowych, które w większości wypadków prowadzą do znacznej i głębokiej niepełnosprawności ruchowej oraz znacząco ograniczają możliwość komunikacji z otoczeniem.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 820
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [828] => Array
                                                        (
                                                            [id] => 828
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 229
                                                            [name] => c) Zespół Aicardiego to zespół wrodzonych wad genetycznych charakteryzujący się częściowym lub całkowitym brakiem ciała modzelowatego, obecnością zmian w siatkówce i napadów drgawkowych.
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 821
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [829] => Array
                                                        (
                                                            [id] => 829
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 229
                                                            [name] => d) Letalne dysplazje kostne u płodu, takie jak dysplazja tanatoforyczna oraz wrodzona łamliwości kości typu III odpowiedzialne są za przyczynę utraty ciąży.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 822
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [230] => Array
                                        (
                                            [id] => 230
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Oznaczenie płci płodu jest konieczne w przypadku diagnostyki prenatalnej: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [830] => Array
                                                        (
                                                            [id] => 830
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 230
                                                            [name] => a) Mukowiscydozy
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 823
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [831] => Array
                                                        (
                                                            [id] => 831
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 230
                                                            [name] => b) Zespołu duplikacji MECP2
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 824
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [832] => Array
                                                        (
                                                            [id] => 832
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 230
                                                            [name] => c) Rdzeniowego zaniku mięśni
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 825
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [833] => Array
                                                        (
                                                            [id] => 833
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 230
                                                            [name] => d) Zespołu Angelmana
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 826
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [231] => Array
                                        (
                                            [id] => 231
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Do Poradni Genetycznej zgłosiła się 25-letnia kobieta z potwierdzonym molekularnie przedwczesnym wygasaniem czynności jajników związanym z FraX (premutacja w genie FMR1) w celu ewentualnej diagnostyki prenatalnej. Do przeprowadzenia badania wykorzystana zostanie technika:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [834] => Array
                                                        (
                                                            [id] => 834
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 231
                                                            [name] => a) PCR z analizą GeneScan i/lub Triplet-Primed PCR (TP-PCR)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 827
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [835] => Array
                                                        (
                                                            [id] => 835
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 231
                                                            [name] => b) Sekwencjonowanie następnej generacji celowane
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 828
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [836] => Array
                                                        (
                                                            [id] => 836
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 231
                                                            [name] => c) Sekwencjonowanie techniką Sangera genu FMR1
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 829
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [837] => Array
                                                        (
                                                            [id] => 837
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 231
                                                            [name] => d) Pacjentce nie powinno się wykonywać diagnostyki prenatalnej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 830
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [232] => Array
                                        (
                                            [id] => 232
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Ryzyko otrzymania wyniku fałszywie pozytywnego dla trisomii w badaniu przesiewowym z wykorzystaniem wolnego płodowego DNA rośnie w przypadku:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [838] => Array
                                                        (
                                                            [id] => 838
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 232
                                                            [name] => a) „vanishing twin”
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 831
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [839] => Array
                                                        (
                                                            [id] => 839
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 232
                                                            [name] => b) Nieprawidłowości chromosomowych u matki
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 832
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [840] => Array
                                                        (
                                                            [id] => 840
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 232
                                                            [name] => c) Mozaikowości
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 833
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [841] => Array
                                                        (
                                                            [id] => 841
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 232
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 834
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [233] => Array
                                        (
                                            [id] => 233
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Ryzyko otrzymania wyniku fałszywie negatywnego dla trisomii w badaniu przesiewowym z wykorzystaniem wolnego płodowego DNA rośnie w przypadku:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [842] => Array
                                                        (
                                                            [id] => 842
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 233
                                                            [name] => a) Aberracja obecna jedynie w komórkach płodu, brak w trofoblaście (TFM ang. true fetal mosaicism)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 835
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [843] => Array
                                                        (
                                                            [id] => 843
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 233
                                                            [name] => b) Zbyt niski % frakcji płodowego DNA (>4%)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 836
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [844] => Array
                                                        (
                                                            [id] => 844
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 233
                                                            [name] => c) Złe przechowywanie próbek z krwią pacjentek
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 837
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [845] => Array
                                                        (
                                                            [id] => 845
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 233
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 838
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [234] => Array
                                        (
                                            [id] => 234
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Podczas badania całoeksomowego badamy:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [846] => Array
                                                        (
                                                            [id] => 846
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 234
                                                            [name] => a) Wszystkie części kodujące genomu
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 839
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [847] => Array
                                                        (
                                                            [id] => 847
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 234
                                                            [name] => b) Kilka lub kilkanaście wybranych genów
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 840
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [848] => Array
                                                        (
                                                            [id] => 848
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 234
                                                            [name] => c) Części niekodujące genomu
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 841
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [849] => Array
                                                        (
                                                            [id] => 849
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 234
                                                            [name] => d) Wszystkie powyżej
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 842
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [250] => Array
                                        (
                                            [id] => 250
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 23
                                            [type_id] => 1
                                            [name] => Celem analizy rodowodu są poniższe stwierdzenia oprócz:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [906] => Array
                                                        (
                                                            [id] => 906
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 250
                                                            [name] => a) ocena rozmieszczenia cech genetycznych w rodzinie
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 899
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [907] => Array
                                                        (
                                                            [id] => 907
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 250
                                                            [name] => b) ocena zróżnicowanej ekspresji choroby u różnych członków rodziny
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                                                            [sort] => 906
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                                                            [status_code] => active
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                                                            [status_code] => active
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                                                            [status_code] => active
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                                                            [ext] => 
                                                            [sort] => 917
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                                                            [ext] => 
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                                                            [status_code] => active
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                                                            [sort] => 919
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                                                            [status_code] => active
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                                                            [sort] => 920
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                                                            [ext] => 
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                                                            [ext] => 
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                                                            [name] => d) występuje z częstością 1 na 500 mężczyzn
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                                                            [ext] => 
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                                                            [status_code] => active
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                                                            [sort] => 255
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [263] => Array
                                                        (
                                                            [id] => 263
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 75
                                                            [name] => c. Występuje w bazie  DGV (The Database of Genomic Variants) jako częsty wariant w populacji
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 256
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [264] => Array
                                                        (
                                                            [id] => 264
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 75
                                                            [name] => d. Została opisana w literaturze i zgłoszona jest do bazy danych DECIPHER
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 257
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [76] => Array
                                        (
                                            [id] => 76
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 41
                                            [type_id] => 1
                                            [name] => W rodzinie w trzech pokoleniach występuje delecja na chromosomie 15 pary. Jednak nie wszyscy nosiciele tej samej zmiany mają nieprawidłowy fenotyp. Jak należy zakwalifikować delecję: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [265] => Array
                                                        (
                                                            [id] => 265
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 76
                                                            [name] => a. Jako wariant łagodny
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 258
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [266] => Array
                                                        (
                                                            [id] => 266
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 76
                                                            [name] => b. Jako zmiana o zmiennej ekspresji
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 259
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [267] => Array
                                                        (
                                                            [id] => 267
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 76
                                                            [name] => c. Jako zmiana o niepełnej penetracji
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 260
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [268] => Array
                                                        (
                                                            [id] => 268
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 76
                                                            [name] => d. Jako zmiana o nieznanym znaczeniu klinicznym
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 261
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [77] => Array
                                        (
                                            [id] => 77
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 41
                                            [type_id] => 1
                                            [name] => Warianty polimorficzne, widoczne w kariotypie klasycznym, takie jak np 1qh+/qh- opisujemy w wyniku:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [269] => Array
                                                        (
                                                            [id] => 269
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 77
                                                            [name] => a. nie umieszczamy ich w wyniku
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 262
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [270] => Array
                                                        (
                                                            [id] => 270
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 77
                                                            [name] => b. umieszczamy takie zmiany w wyniki ale nie dodajemy słowa "nieprawidłowy"
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 263
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [271] => Array
                                                        (
                                                            [id] => 271
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 77
                                                            [name] => c. jako prawdopodobnie patogenne
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 264
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [272] => Array
                                                        (
                                                            [id] => 272
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 77
                                                            [name] => d. umieszczamy w wyniku opisując jako "zmiany łagodne" lub "zmiany niemające wpływu na fenotyp"
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 265
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [78] => Array
                                        (
                                            [id] => 78
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 41
                                            [type_id] => 1
                                            [name] => Kariotyp konwencjonalny pacjenta, który został skierowany na badanie z podejrzeniem Zespołu Downa, powinien zostać wykonany przy minimalnej rozdzielczości:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [273] => Array
                                                        (
                                                            [id] => 273
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 78
                                                            [name] => a. 200 prążków
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 266
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [274] => Array
                                                        (
                                                            [id] => 274
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 78
                                                            [name] => b. 300 prążków
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 267
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [275] => Array
                                                        (
                                                            [id] => 275
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 78
                                                            [name] => c. 400 prążków
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 268
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [276] => Array
                                                        (
                                                            [id] => 276
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 78
                                                            [name] => d. 550 prążków
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 269
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [79] => Array
                                        (
                                            [id] => 79
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 41
                                            [type_id] => 1
                                            [name] => Kariotyp mężczyzny, nosiciela fuzji robertsonowskiej między chromosomami 13 i 14 pary zapisujemy: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [277] => Array
                                                        (
                                                            [id] => 277
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 79
                                                            [name] => a. 46,XY,t(13;14)(q10;q10)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 270
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [278] => Array
                                                        (
                                                            [id] => 278
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 79
                                                            [name] => b. 45,XY,der(13;14)(q10;q10)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 271
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [279] => Array
                                                        (
                                                            [id] => 279
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 79
                                                            [name] => c. 46,XY,der(13;14)(q10;q10)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 272
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [280] => Array
                                                        (
                                                            [id] => 280
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 79
                                                            [name] => d. 45,XY,der(14;13)(q10;q10)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 273
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [80] => Array
                                        (
                                            [id] => 80
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 41
                                            [type_id] => 1
                                            [name] => Pacjentka z wynikiem badania: 46,XX,inv(12)(p13.32q24.31) ma kariotyp: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [281] => Array
                                                        (
                                                            [id] => 281
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 80
                                                            [name] => a. nieprawidłowy niezrównoważony
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 274
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [282] => Array
                                                        (
                                                            [id] => 282
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 80
                                                            [name] => b. prawidłowy zrównoważony
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 275
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [283] => Array
                                                        (
                                                            [id] => 283
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 80
                                                            [name] => c. prawidłowy niezrównoważony
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 276
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [284] => Array
                                                        (
                                                            [id] => 284
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 80
                                                            [name] => d. nieprawidłowy zrównoważony
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 277
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [81] => Array
                                        (
                                            [id] => 81
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 41
                                            [type_id] => 2
                                            [name] => Programem przydatnym dla weryfikacji poprawności zapisu mutacji jest: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [285] => Array
                                                        (
                                                            [id] => 285
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 81
                                                            [name] => a. Mutalyzer
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 278
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [286] => Array
                                                        (
                                                            [id] => 286
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 81
                                                            [name] => b. ClinVar
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 279
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [287] => Array
                                                        (
                                                            [id] => 287
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 81
                                                            [name] => c. Ensembl
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 280
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [288] => Array
                                                        (
                                                            [id] => 288
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 81
                                                            [name] => d. GeneMarker
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 281
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [82] => Array
                                        (
                                            [id] => 82
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 41
                                            [type_id] => 1
                                            [name] => U pacjenta z podejrzeniem hipolplazji mostu i móżdżku typu 1B (dziedziczenie autosomalne recesywne) zidentyfikowano homozygotyczną mutację c.92G>C (p.Gly31Ala). Nie badano jej dziedziczenia od rodziców. Prawidłowy zapis genotypu Pacjenta zgodny z HGVS będzie następujący: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [289] => Array
                                                        (
                                                            [id] => 289
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 82
                                                            [name] => a. NM_016042.4:c.(92G>C);(92G>C); NP_057126.2:p.(Gly31Ala);(Gly31Ala)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 282
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [290] => Array
                                                        (
                                                            [id] => 290
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 82
                                                            [name] => b. NM_016042.4:c.[92G>C];[92G>C]; NP_057126.2:p.[Gly31Ala];[Gly31Ala]
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 283
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [291] => Array
                                                        (
                                                            [id] => 291
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 82
                                                            [name] => c. NM_016042.4:c.92G>C(;)(92G>C); NP_057126.2:p.Gly31Ala(;)(Gly31Ala)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 284
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [292] => Array
                                                        (
                                                            [id] => 292
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 82
                                                            [name] => d. NM_016042.4:c.92G>C/92G>C; NP_057126.2:p.Gly31Ala/Gly31Ala
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 285
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [83] => Array
                                        (
                                            [id] => 83
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 41
                                            [type_id] => 1
                                            [name] => Która z niżej wymienionych biologicznych baz danych jest bazą populacyjną, zawierającą informacje o częstości występowania wariantów w populacji:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [293] => Array
                                                        (
                                                            [id] => 293
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 83
                                                            [name] => a. OMIM
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 286
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [294] => Array
                                                        (
                                                            [id] => 294
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 83
                                                            [name] => b. gnomAD
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 287
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [295] => Array
                                                        (
                                                            [id] => 295
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 83
                                                            [name] => c. SRA
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 288
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [296] => Array
                                                        (
                                                            [id] => 296
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 83
                                                            [name] => d. GenBank
                                                            [correct] => 0
                                                            [ext] => 
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                                            [name] => Aby móc prawidłowo zinterpretować wynik badania otrzymany metodą mikromacierzy należy: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [129] => Array
                                                        (
                                                            [id] => 129
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 37
                                                            [name] => a. Wykonać dodatkowe badanie techniką FISH
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 122
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [130] => Array
                                                        (
                                                            [id] => 130
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 37
                                                            [name] => b. Ustalić rodzicielskie pochodzenie stwierdzonej zmiany oraz sprawdzić, czy dana zmiana nie została opisana w bazie danych Database of Genomic Variants
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 123
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [131] => Array
                                                        (
                                                            [id] => 131
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 37
                                                            [name] => c. Ustalić rodzicielskie pochodzenie stwierdzonej zmiany oraz sprawdzić, czy dana zmiana nie została opisana w bazie DECIPHER.
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 124
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [132] => Array
                                                        (
                                                            [id] => 132
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 37
                                                            [name] => d. Ustalić rodzicielskie pochodzenie stwierdzonej zmiany oraz sprawdzić, czy została ona opisana w bazie wariantów polimorficznych lub w bazie wariantów patogennych.
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 125
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [38] => Array
                                        (
                                            [id] => 38
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 42
                                            [type_id] => 2
                                            [name] => Zmianę CNV, stwierdzona za pomocą techniki mikromacierzy CGH, możemy określić jako patogenną tylko jeśli: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [133] => Array
                                                        (
                                                            [id] => 133
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 38
                                                            [name] => a. Powstała de novo
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 126
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [134] => Array
                                                        (
                                                            [id] => 134
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 38
                                                            [name] => b. Jest pochodzenia rodzicielskiego
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 127
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [135] => Array
                                                        (
                                                            [id] => 135
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 38
                                                            [name] => c. Występuje w bazie  DGV (The Database of Genomic Variants) jako częsty wariant w populacji
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 128
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [136] => Array
                                                        (
                                                            [id] => 136
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 38
                                                            [name] => d. Została opisana w literaturze i zgłoszona jest do bazy danych DECIPHER
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 129
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [39] => Array
                                        (
                                            [id] => 39
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 42
                                            [type_id] => 1
                                            [name] => Zmianę CNV, stwierdzona za pomocą techniki mikromacierzy CGH, możemy określić jako łagodną tylko jeśli: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [137] => Array
                                                        (
                                                            [id] => 137
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 39
                                                            [name] => a. Powstała de novo
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 130
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [138] => Array
                                                        (
                                                            [id] => 138
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 39
                                                            [name] => b. Jest pochodzenia rodzicielskiego
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 131
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [139] => Array
                                                        (
                                                            [id] => 139
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 39
                                                            [name] => c. Występuje w bazie  DGV (The Database of Genomic Variants) jako częsty wariant w populacji
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 132
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [140] => Array
                                                        (
                                                            [id] => 140
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 39
                                                            [name] => d. Została opisana w literaturze i zgłoszona jest do bazy danych DECIPHER
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 133
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [40] => Array
                                        (
                                            [id] => 40
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 42
                                            [type_id] => 1
                                            [name] => W rodzinie w trzech pokoleniach występuje delecja na chromosomie 15 pary. Jednak nie wszyscy nosiciele tej samej zmiany mają nieprawidłowy fenotyp. Jak należy zakwalifikować delecję: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [141] => Array
                                                        (
                                                            [id] => 141
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 40
                                                            [name] => a. Jako wariant łagodny
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 134
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [142] => Array
                                                        (
                                                            [id] => 142
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 40
                                                            [name] => b. Jako zmiana o zmiennej ekspresji
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 135
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [143] => Array
                                                        (
                                                            [id] => 143
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 40
                                                            [name] => c. Jako zmiana o niepełnej penetracji
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 136
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [144] => Array
                                                        (
                                                            [id] => 144
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 40
                                                            [name] => d. Jako zmiana o nieznanym znaczeniu klinicznym
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 137
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [41] => Array
                                        (
                                            [id] => 41
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 42
                                            [type_id] => 1
                                            [name] => Warianty polimorficzne, widoczne w kariotypie klasycznym, takie jak np 1qh+/qh- opisujemy w wyniku:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [145] => Array
                                                        (
                                                            [id] => 145
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 41
                                                            [name] => a. nie umieszczamy ich w wyniku
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 138
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [146] => Array
                                                        (
                                                            [id] => 146
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 41
                                                            [name] => b. umieszczamy takie zmiany w wyniki ale nie dodajemy słowa "nieprawidłowy"
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 139
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [147] => Array
                                                        (
                                                            [id] => 147
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 41
                                                            [name] => c. jako prawdopodobnie patogenne
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 140
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [148] => Array
                                                        (
                                                            [id] => 148
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 41
                                                            [name] => d. umieszczamy w wyniku opisując jako "zmiany łagodne" lub "zmiany niemające wpływu na fenotyp"
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 141
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [42] => Array
                                        (
                                            [id] => 42
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 42
                                            [type_id] => 1
                                            [name] => Kariotyp konwencjonalny pacjenta, który został skierowany na badanie z podejrzeniem Zespołu Downa, powinien zostać wykonany przy minimalnej rozdzielczości:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [149] => Array
                                                        (
                                                            [id] => 149
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 42
                                                            [name] => a. 200 prążków
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 142
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [150] => Array
                                                        (
                                                            [id] => 150
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 42
                                                            [name] => b. 300 prążków
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 143
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [151] => Array
                                                        (
                                                            [id] => 151
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 42
                                                            [name] => c. 400 prążków
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 144
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [152] => Array
                                                        (
                                                            [id] => 152
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 42
                                                            [name] => d. 550 prążków
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 145
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [43] => Array
                                        (
                                            [id] => 43
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 42
                                            [type_id] => 1
                                            [name] => Kariotyp mężczyzny, nosiciela fuzji robertsonowskiej między chromosomami 13 i 14 pary zapisujemy: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [153] => Array
                                                        (
                                                            [id] => 153
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 43
                                                            [name] => a. 46,XY,t(13;14)(q10;q10)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 146
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [154] => Array
                                                        (
                                                            [id] => 154
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 43
                                                            [name] => b. 45,XY,der(13;14)(q10;q10)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 147
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [155] => Array
                                                        (
                                                            [id] => 155
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 43
                                                            [name] => c. 46,XY,der(13;14)(q10;q10)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 148
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [156] => Array
                                                        (
                                                            [id] => 156
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 43
                                                            [name] => d. 45,XY,der(14;13)(q10;q10)
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 149
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [44] => Array
                                        (
                                            [id] => 44
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 42
                                            [type_id] => 1
                                            [name] => Pacjentka z wynikiem badania: 46,XX,inv(12)(p13.32q24.31) ma kariotyp: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
                                                    [157] => Array
                                                        (
                                                            [id] => 157
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 44
                                                            [name] => a. nieprawidłowy niezrównoważony
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 150
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [158] => Array
                                                        (
                                                            [id] => 158
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 44
                                                            [name] => b. prawidłowy zrównoważony
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 151
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [159] => Array
                                                        (
                                                            [id] => 159
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 44
                                                            [name] => c. prawidłowy niezrównoważony
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 152
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [160] => Array
                                                        (
                                                            [id] => 160
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 44
                                                            [name] => d. nieprawidłowy zrównoważony
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 153
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

                                    [45] => Array
                                        (
                                            [id] => 45
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 42
                                            [type_id] => 2
                                            [name] => Programem przydatnym dla weryfikacji poprawności zapisu mutacji jest: 
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => wielokrotna odpowiedź
                                            [type_code] => multi
                                            [answers] => Array
                                                (
                                                    [161] => Array
                                                        (
                                                            [id] => 161
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 45
                                                            [name] => a. Mutalyzer
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 154
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                    [162] => Array
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                                                            [name] => d. GeneMarker
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                                            [type_id] => 1
                                            [name] => U pacjenta z podejrzeniem hipolplazji mostu i móżdżku typu 1B (dziedziczenie autosomalne recesywne) zidentyfikowano homozygotyczną mutację c.92G>C (p.Gly31Ala). Nie badano jej dziedziczenia od rodziców. Prawidłowy zapis genotypu Pacjenta zgodny z HGVS będzie następujący:
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                                                            [ext] => 
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                                                            [ext] => 
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                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 612
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

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                                                        (
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                                                            [name] => d. NM_016042.4:c.92G>C/92G>C; NP_057126.2:p.Gly31Ala/Gly31Ala
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                                                            [ext] => 
                                                            [sort] => 613
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                                                            [status_code] => active
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                                                        )

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                                            [name] => Która z niżej wymienionych biologicznych baz danych jest bazą populacyjną, zawierającą informacje o częstości występowania wariantów w populacji:
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                                                            [status_name] => Aktywny
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                                                            [ext] => 
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                                                            [status_name] => Aktywny
                                                            [status_code] => active
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                                                        (
                                                            [id] => 624
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                                                            [question_id] => 177
                                                            [name] => d. GenBank
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                                                            [ext] => 
                                                            [sort] => 617
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
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                                            [name] => Jakiego rodzaju informacji NIE znajdziemy w bazie OMIM
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                                                            [status_name] => Aktywny
                                                            [status_code] => active
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                                                            [ext] => 
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                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                            [name] => W badaniu eksomu stosuje się filtr częstości, aby
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                                            [sort] => 0
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                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
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                                                            [id] => 629
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                                                            [status_id] => 5
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                                                            [name] => a. wyłączyć z analizy warianty polimorficzne, a pozostawić rzadkie, potencjalnie patogenne
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                                                            [ext] => 
                                                            [sort] => 622
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                        (
                                                            [id] => 630
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 179
                                                            [name] => b. ocenić jakość sekwencjonowania
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 623
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

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                                                            [id] => 631
                                                            [site_id] => 1
                                                            [status_id] => 5
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                                                            [name] => c. wykonać analizę dziedziczenia
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 624
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

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                                                        (
                                                            [id] => 632
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                                                            [name] => d. ocenić konformację zmutowanego białka
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                                                            [ext] => 
                                                            [sort] => 625
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                )

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                                            [type_id] => 1
                                            [name] => W badaniach genomowych metodą NGS wyróżniamy:
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                                            [status_code] => active
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                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 626
                                                            [correct_yesno] => Nie
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                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
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                                                            [name] => b. sekwencjonowanie panelowe, sekwencjonowanie eksomowe (WES) i sekwencjonowanie genomowe (WGS)
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 627
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

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                                                        (
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                                                            [status_id] => 5
                                                            [question_id] => 180
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                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 628
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [636] => Array
                                                        (
                                                            [id] => 636
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 180
                                                            [name] => d. sekwencjonowanie de novo, sekwencjonowanie przez syntezę, sekwencjonowanie sangerowskie
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 629
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

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                                        (
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                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 43
                                            [type_id] => 1
                                            [name] => Warianty de novo, to warianty, które:
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
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                                                (
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                                                        (
                                                            [id] => 637
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 181
                                                            [name] => a. zidentyfikowano w nowych, nie opisanych dotąd genach
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 630
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [638] => Array
                                                        (
                                                            [id] => 638
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 181
                                                            [name] => b. odnoszą się do nowych, nie opisanych dotąd mutacji
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 631
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [639] => Array
                                                        (
                                                            [id] => 639
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 181
                                                            [name] => c. nie są odziedziczone po rodzicach
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 632
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [640] => Array
                                                        (
                                                            [id] => 640
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 181
                                                            [name] => d. są odziedziczone po obojgu rodzicach
                                                            [correct] => 0
                                                            [ext] => 
                                                            [sort] => 633
                                                            [correct_yesno] => Nie
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                )

                                        )

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                                        (
                                            [id] => 182
                                            [site_id] => 1
                                            [status_id] => 5
                                            [group_id] => 43
                                            [type_id] => 1
                                            [name] => Wynik badania WES u probanta i analiza rodziców wskazuje na patogenną mutację de novo u probanta. Wynik ten oznacza, że
                                            [ext] => 
                                            [sort] => 0
                                            [status_name] => Aktywny
                                            [status_code] => active
                                            [status_admin] => #1Aktywny
                                            [type_name] => pojedyncza odpowiedź
                                            [type_code] => single
                                            [answers] => Array
                                                (
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                                                        (
                                                            [id] => 641
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 182
                                                            [name] => a. rodzice nie są nosicielami mutacji, ale nie wyklucza to istnienia mozaikowości germinalnej i ryzyka przekazania mutacji kolejnemu dziecku
                                                            [correct] => 1
                                                            [ext] => 
                                                            [sort] => 634
                                                            [correct_yesno] => Tak
                                                            [status_name] => Aktywny
                                                            [status_code] => active
                                                            [status_admin] => #1Aktywny
                                                        )

                                                    [642] => Array
                                                        (
                                                            [id] => 642
                                                            [site_id] => 1
                                                            [status_id] => 5
                                                            [question_id] => 182
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