Mukowiscydoza (CF) jest wywoływana przez gen, który nie działa prawidłowo. Dowiedz się, co badania genetyczne mogą powiedzieć Ci o tym wadliwym genie i jakie mogą być Twoje dalsze kroki.
Refluks pęcherzowo-moczowodowy to sytuacja, w której mocz wypływa z powrotem z pęcherza. Może on potencjalnie cofnąć się do nerek, co może spowodować ich uszkodzenie. Choroba ta występuje zwykle u niemowląt i małych dzieci, a większość z nich jest w stanie z niej zrezygnować.
Zespół Noonan jest chorobą genetyczną, która powoduje wady serca, problemy z krwawieniem, wyraźne rysy twarzy i inne. Lekarz informuje, jakich objawów należy szukać u niemowląt i dzieci.
Ubytek słuchu u niemowląt jest trudny do wykrycia. Dowiedz się od lekarza, jak bada się słuch noworodków i co robić, jeśli Twoje dziecko może mieć ubytek słuchu.
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