Conditions / Genetic
spinocerebellar ataxia 15
info · Genetic
An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, nystagmus, dysarthria and dysphagia, has_material_basis_in mutation in the ITPR1 gene.
Signs and symptoms
- Cerebellar atrophy
- Impaired tandem gait
- Gait ataxia
- Intention tremor
- Nystagmus
- Cerebellar cortical atrophy
- Cerebellar vermis atrophy
- Broad-based gait
- Truncal ataxia
- Gait disturbance
Also known as: spinocerebellar ataxia type 16