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Up to: Autosomal dominant cerebellar ataxia type I
Spinocerebellar ataxia type 36
Spinocerebellar ataxia type 36 (SCA36) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasiculations, tongue atrophy and hyperreflexia.
This condition has no sub-types.