Синдром KBG
ORPHA:2332· ICD-10 Q87.8· KBG syndrome
Визначення(English summary)
A rare congenital malformation syndrome characterized by a typical facial dysmorphism, macrodontia of the permanent upper central incisors, short stature, skeletal anomalies, developmental delay and behavioral abnormalities.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal dominant
- Вік початку
- Adolescent, Childhood, Infancy, Neonatal