Conditions / Genetic
spinocerebellar ataxia 30
info · Genetic
An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene.
Signs and symptoms
- Cerebellar atrophy
- Dysarthria
- Ataxia
- Hypermetric saccades
- Gaze-evoked nystagmus