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Up to: Huntington disease-like syndrome · Autosomal dominant cerebellar ataxia type IV
Dentatorubral-pallidoluysian atrophy
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.
This condition has no sub-types.