Spinocerebellar ataxia 14
Overview
Spinocerebellar ataxia 14: A rare genetic disorder (chromosome 19q13.4qter defect) characterized by gait ataxia, tremors and dysarthria (speech disorder). The condition progresses slowly.
Symptoms
Gait ataxia Dysarthria Tremor Limb ataxia Myoclonus
Diagnosis
The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Spinocerebellar ataxia 14. This medical information about signs and symptoms for Spinocerebellar ataxia 14 has been gathered from various sources, may not be fully accurate, and may not be the full list of Spinocerebellar ataxia 14 signs or Spinocerebellar ataxia 14 symptoms. Furthermore, signs and symptoms of Spinocerebellar ataxia 14 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 14 symptoms.