Noonan Syndrome 누난 증후군 Noonan syndrome is an autosomal dominant disorder with a prevalence of 1 in 1000 to 2500 live births (20).The syndrome, which affects both sexes equally, is characterized by dysmorphic facies, short stature, webbed neck, skeletal deformities, cryptorchidism, bleeding diatheses, and cardiac anomalies (20).Cardiac involvement is observed in 80% to 90% of affected fetuses, with valvular pulmonary s.. 2024. 7. 11. 이전 1 다음
