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Genetic and Rare Diseases Information Center (GARD)

Spinocerebellar ataxia


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How might spinocerebellar ataxia be treated?

There is no known cure for spinocerebellar ataxia (SCA). The best treatment options for SCA vary by type and often depend on the signs and symptoms present in each person. The most common symptom of SCA is problems with coordination and balance (ataxia). Physical therapy can help strengthen muscles, while special devices (a cane, crutches, walker or wheelchair) can assist in mobility and other activities of daily life.[1] Many people with SCA have other symptoms in addition to the ataxia. Medications or other therapies may be suggested for some of these symptoms such as tremor, stiffness, muscle spasms, and sleep disorders.[2]
Last updated: 12/3/2014

  1. NINDS Ataxias and Cerebellar or Spinocerebellar Degeneration Information Page. National Institute of Neurological Disorders and Stroke. April 2014;
  2. Autosomal Dominant Hereditary Ataxia. NORD. April 2014;

Management Guidelines

  • GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions.

Clinical Trials & Research for this Disease

  • lists trials that are studying or have studied Spinocerebellar ataxia. Click on the link to go to to read descriptions of these studies.
Other Names for this Disease
  • SCA
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