Conditions / Genetic
cerebellar ataxia type 41
info · Genetic
An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the TRPC3 gene on chromosome 4q27.
Signs and symptoms
- Gait ataxia
- Postural instability
- Unsteady gait
- Cerebellar vermis atrophy
- Cerebellar atrophy
- Ataxia
Also known as: SCA41