Хвороба Менкеса
ORPHA:565· ICD-10 E83.0· Menkes disease
Визначення(English summary)
A rare congenital disorder of copper metabolism with severe multisystemic manifestations that are primarily characterized by progressive neurodegeneration and marked connective tissue anomalies. A pathognomonic feature is the typical sparse, abnormal steely hair.
- Поширеність
- Unknown
- Успадкування
- X-linked recessive
- Вік початку
- Neonatal