Spinocerebellar ataxia type 41

Spinocerebellar ataxia type 41 is a rare autosomal dominant cerebellar ataxia type III disorder characterized by adult-onset progressive imbalance and loss of coordination associated with an ataxic gait. Mild atrophy of the cerebellar vermis has been reported on brain magnetic resonance imaging.

Also known as: SCA41, spinocerebellar ataxia type 41, spinocerebellar ataxia 41

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 41 itself.