Spinocerebellar ataxia 20
Overview
Spinocerebellar ataxia 20: A rare genetic disorder (chromosome 11 defect) characterized by palatal tremor and dysphonia. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types.
Symptoms
Gait ataxia Mild sensory neuropathy Speech problems Dysphonia Ataxia
Diagnosis
The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Spinocerebellar ataxia 20. This medical information about signs and symptoms for Spinocerebellar ataxia 20 has been gathered from various sources, may not be fully accurate, and may not be the full list of Spinocerebellar ataxia 20 signs or Spinocerebellar ataxia 20 symptoms. Furthermore, signs and symptoms of Spinocerebellar ataxia 20 may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Spinocerebellar ataxia 20 symptoms.