Conditions / Genetic
autosomal recessive spinocerebellar ataxia 10
info · Genetic
An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene.
Signs and symptoms
- Cerebellar atrophy
- Dysarthria
- Gait ataxia
- Limb ataxia
- Hyperactive Achilles reflex
- Hyperactive patellar reflex
- Upper limb hyperreflexia
- Nystagmus
- Hypermetric saccades
- Truncal ataxia
Also known as: SCAR10