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Up to: Autosomal dominant cerebellar ataxia type I
Spinocerebellar ataxia type 29
Spinocerebellar ataxia type 29 (SCA29) is a rare subtype of autosomal dominant cerebellar ataxia type I (ADCA type I) characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.
This condition has no sub-types.