Spinocerebellar ataxia type 29

Spinocerebellar ataxia type 29 (SCA29) is a rare subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1; see this term) characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.

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Aliases

• ACV
• aplasia of cerebellar vermis
• cerebellar ataxia early-onset nonprogressive
• cerebellar ataxia, congenital nonprogressive, autosomal dominant
• cerebellar vermis aplasia
• Congenital nonprogressive spinocerebellar ataxia
• congenital nonprogressive spinocerebellar ataxia
• SCA29
• spinocerebellar ataxia 29
• spinocerebellar ataxia type 29
• spinocerebellar ataxia type 29