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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