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Up to: Huntington disease-like syndrome · Autosomal dominant cerebellar ataxia type I
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities.
This condition has no sub-types.