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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