Spinocerebellar ataxia type 40

Spinocerebellar ataxia type 40 (SCA40) is a very rare subtype of autosomal dominant cerebellar ataxia type 1, characterized by the adult-onset of unsteady gait and dysarthria, followed by wide-based gait, gait ataxia, ocular dysmetria, intention tremor, scanning speech, hyperreflexia and dysdiadochokinesis.

Also known as: SCA40, spinocerebellar ataxia type 40, spinocerebellar ataxia 40

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 40 itself.