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Up to: Autosomal dominant cerebellar ataxia type I
Spinocerebellar ataxia type 4
Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by ataxia with sensory neuropathy.
This condition has no sub-types.