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Хвороба Гантінгтон-подібна 2

ORPHA:98934· ICD-10 G10· Huntington disease-like 2

Визначення(English summary)

A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia).

Поширеність
<1 / 1 000 000
Успадкування
Autosomal dominant
Вік початку
Adult