Conditions / Genetic
spinocerebellar ataxia 10
info · Genetic
An autosomal dominant cerebellar ataxia that is characterized by gait ataxia, upper-limb ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the ATXN10 gene.
Signs and symptoms
- Polyneuropathy
- Gait ataxia
- Dysarthria
- Limb ataxia
- Scanning speech
- Bradykinesia
- Dysmetria
- Seizure
- Cerebellar atrophy
- Urinary incontinence