Spinocerebellar ataxia type 41

MONDO:0014626

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

172 clinical trials for this condition and its sub-types.

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