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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Friedreich ataxia


Other Names for this Disease

  • FRDA
  • Friedreich's ataxia
  • Hereditary spinal ataxia
  • Hereditary spinal sclerosis
  • Spinocerebellar ataxia, Friedreich
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Your Question

My daughter has Friedreich ataxia. Both of her parents are black, and her paternal great grandmother is of Irish descent. How did my daughter inherit this condition, and how can I find other families that are in a similar situation?

Our Answer

We have identified the following information that we hope you find helpful. If you still have questions, please contact us.

How is Friedreich ataxia inherited?

Friedreich ataxia is inherited in an autosomal recessive pattern, which means that both copies of the FXN gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene (and are referred to as carriers); but they typically do not show signs and symptoms of the condition. When two people who are carriers of an autosomal recessive condition have a child, each time there is a 25% (1 in 4) chance that the child will have the condition, a 50% (1 in 2) chance that the child will be a carrier like each of the parents, and a 25% (1 in 4) chance that the child will not have the condition and not be a carrier.[1]
Last updated: 1/23/2012

Can Friedreich ataxia affect individuals of any ethnicity?

Some genetic disorders are more likely to occur among people who trace their ancestry to a particular geographic area. People in an ethnic group often share certain versions of their genes, which have been passed down from common ancestors. If one of these shared genes contains a disease-causing mutation, a particular genetic disorder may be more frequently seen in the group.[2] Although rare, Friedreich ataxia is the most common form of hereditary ataxia, affecting about 1 in every 50,000 people in the United States.[3] This condition is typically found in people with European, Middle Eastern, or North African ancestry and it is rarely identified in other ethnic groups.[4] There have been no reports of individuals with Friedreich ataxia in Southeast Asia, in sub-Saharan Africa, or among Native Americans.[5] About 1 in 100 Americans are Friedreich ataxia carriers, but in some ethnic groups the frequency is higher. For example, about one in 70 people of Acadian (Cajun) ancestry are carriers.[6]
Last updated: 12/13/2010

How can I find other families with Freidreich ataxia that are in a similar situation?

The Friedreich's Ataxia Parents' Group, an online support group, is an international group that includes parents and guardians of children with this condition and other childhood-onset ataxias. This website provides a forum to share unique experiences and knowledge of how individuals have learned to cope with ataxia in their families.

There are also Parent Matching Organizations such as Madisons Foundation and MUMS, which connect parents whose children have the same disease.

To view a list of resources for individuals and families with Friedreich ataxia (including the support groups mentioned above), click here.
Last updated: 12/13/2010

References
Other Names for this Disease
  • FRDA
  • Friedreich's ataxia
  • Hereditary spinal ataxia
  • Hereditary spinal sclerosis
  • Spinocerebellar ataxia, Friedreich
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.