Спадкова хвороба Крейтцфельдта-Якоба
ORPHA:282166· ICD-10 A81.0· Inherited Creutzfeldt-Jakob disease
Визначення(English summary)
A rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal dominant
- Вік початку
- Adult, Elderly