Conditions / Genetic
spinocerebellar ataxia 18
info · Genetic
An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23.
Signs and symptoms
- Hyporeflexia
- Skeletal muscle atrophy
- Dysmetria
- Pes cavus
- Babinski sign
- Cerebellar atrophy
- Areflexia
- Dysdiadochokinesis
- Limb muscle weakness
- Sensory axonal neuropathy