Spinocerebellar ataxia 23
Overview
Spinocerebellar ataxia 23: A rare genetic disorder (chromosome 20p13-12.3 defect) characterized by ataxia, sensory loss and pyramidal signs. It is a slowly progressing condition.
Symptoms
Gait ataxia Mild sensory neuropathy Speech problems Limb ataxia Eye movement problems
Diagnosis
The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Spinocerebellar ataxia 23. This medical information about signs and symptoms for Spinocerebellar ataxia 23 has been gathered from various sources, may not be fully accurate, and may not be the full list of Spinocerebellar ataxia 23 signs or Spinocerebellar ataxia 23 symptoms. Furthermore, signs and symptoms of Spinocerebellar ataxia 23 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 23 symptoms.