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Up to: Autosomal dominant cerebellar ataxia type I
Spinocerebellar ataxia type 35
Spinocerebellar ataxia type 35 (SCA35) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, intention tremor, hyperreflexia and spasmodic torticollis.
This condition has no sub-types.