Conditions / Genetic
spinocerebellar ataxia 19/22
info ยท Genetic
An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor.
Signs and symptoms
- Cerebellar atrophy
- Gait ataxia
- Dysarthria
- Saccadic smooth pursuit interruptions
- Nystagmus
- Hyporeflexia
- Gaze-evoked horizontal nystagmus
- Truncal ataxia
- Postural tremor
- Progressive cerebellar ataxia