Хвороба Вільсона
ORPHA:905· ICD-10 E83.0· Wilson disease
Визначення(English summary)
A rare genetic disorder of copper metabolism presenting with non-specific hepatic, neurologic, psychiatric or ophthalmologic manifestations due to impaired biliary copper excretion and consecutive excessive copper deposition in the body.
- Поширеність
- 1-9 / 100 000
- Успадкування
- Autosomal recessive
- Вік початку
- Adolescent, Adult, Childhood, Elderly