Conditions / Genetic
spinocerebellar ataxia 35
info · Genetic
An autosomal dominant cerebellar ataxia that is characterized by a slowly progressive ataxia, tremor, dysarthria and hyperreflexia, has_material_basis_in mutation in the TGM6 gene.
Signs and symptoms
- Dysmetria
- Cerebellar atrophy
- Ataxia
- Pseudobulbar paralysis
- Dysarthria
- Hyperreflexia
- Gait disturbance
- Loss of ambulation
- Incoordination
- Neck muscle weakness