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Spinocerebellar ataxia type 2

MONDO:0008458

A subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea.

Also known as: ATXN2 autosomal dominant cerebellar ataxia type I, OPCA2, SCA2, autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2, spinocerebellar ataxia type 2, ALS13, SCA 2, Wadia swami syndrome

38 clinical trials for this condition and its sub-types, 10 tagged with Spinocerebellar ataxia type 2 itself.

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Sub-types of Spinocerebellar ataxia type 2

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