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W badaniu przesiewowym I trymestru w USG wykonanym 12+4 t.c. nie uwidoczniono u płodu kości nosowej. Wynik testu złożone: ryzyko dla trisomii 21 wynosi 1:290, dla pozostałych trisomii ryzyko niskie. Obecnie pacjentka jest w 16 t.c. Jakie badania powinny być zaproponowane pacjentce w pierwszej kolejności?
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