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