Dentatorubral-pallidoluysian atrophy

MONDO:0007435

Dentatorubral pallidoluysian atrophy (DRPLA) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by involuntary movements, ataxia, epilepsy, mental disorders, cognitive decline and prominent anticipation.

Also known as: DRPLA, Dentatorubropallidoluysian atrophy, Naito-Oyanagi disease, dentatorubral-pallidoluysian atrophy, haw River syndrome, NOD, Naito Oyanagi disease, ataxia, chorea, seizures, and dementia

175 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by