Conditions / Genetic
spinocerebellar ataxia 7
info · Genetic
An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene.
Signs and symptoms
- Dysarthria
- Progressive cerebellar ataxia
- Nystagmus
- Tremor
- Hyperreflexia
- Olivopontocerebellar atrophy
- Dysphagia
- Dysmetria
- Orofacial dyskinesia
- Babinski sign