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.

Also known as: SCA29, congenital nonprogressive spinocerebellar ataxia, spinocerebellar ataxia 29, congenital nonprogressive, spinocerebellar ataxia type 29, ACV, aplasia of cerebellar vermis, cerebellar ataxia early-onset nonprogressive, cerebellar ataxia, congenital nonprogressive, autosomal dominant

20 clinical trials for this condition and its sub-types, 1 tagged with Spinocerebellar ataxia type 29 itself.