Вроджена аплазія шкіри
ORPHA:1114· ICD-10 Q84.8· Aplasia cutis congenita
Визначення(English summary)
A rare skin disorder characterized by localized absence of skin that is usually located on the scalp but can occur anywhere on the body including the face, trunk and extremities. Aplasia cutis congenita (ACC) may occasionally be associated with other anomalies.
- Поширеність
- 1-5 / 10 000
- Успадкування
- Autosomal dominant, Autosomal recessive, Not applicable
- Вік початку
- Antenatal, Neonatal