Spinocerebellar ataxia 25

Overview

Spinocerebellar ataxia 25: A rare genetic disorder (chromosome 2p15-p21 defect) characterized by sensory neuropathy and damage to the motor control part of the brain (cerebellar atrophy) resulting in ataxia. It is a slow progressing condition.

Symptoms

Gait ataxia Sensory neuropathy Ataxia Vomiting Gastrointestinal symptoms

Diagnosis

The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Spinocerebellar ataxia 25. This medical information about signs and symptoms for Spinocerebellar ataxia 25 has been gathered from various sources, may not be fully accurate, and may not be the full list of Spinocerebellar ataxia 25 signs or Spinocerebellar ataxia 25 symptoms. Furthermore, signs and symptoms of Spinocerebellar ataxia 25 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 25 symptoms.