Conditions / Genetic
spinocerebellar ataxia 26
info · Genetic
An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and oculomotor abnormalities, has_material_basis_in mutation in the EEF2 gene.
Signs and symptoms
- Incoordination
- Truncal ataxia
- Nystagmus
- Impaired horizontal smooth pursuit
- Cerebellar atrophy
- Dysarthria
- Gait ataxia
- Limb ataxia
- Dysmetric saccades