vitalwiki

Синдром Нунана

ORPHA:648· ICD-10 Q87.1· Noonan syndrome

Визначення(English summary)

A rare, highly variable, multisystemic disorder mainly characterized by short stature, distinctive facial features, congenital heart defects, cardiomyopathy and an increased risk to develop tumors in childhood.

Поширеність
1-5 / 10 000
Успадкування
Autosomal dominant, Autosomal recessive
Вік початку
Antenatal, Childhood, Infancy, Neonatal