Friedreich’s ataxia is a rare, inherited disease. It causes a gradual breakdown of the nervous system. Friedreich’s ataxia affects nerves in the brain and spinal cord that control movement. It also affects sensory nerves that help with coordination. In later stages, the disease can cause injury to the heart and pancreas.
|The Nervous System|
|Copyright © Nucleus Medical Media, Inc.|
Friedreich’s ataxia is caused by a problem with a gene called the frataxin gene. This gene is found on chromosome 9q13. To develop this disease, a person must inherit a copy of the defective gene from each parent. However, there are some people with Friedreich’s ataxia that have no family history of the disorder.
There are no known risk factors other than having a parent with the frataxin gene.
Symptoms can be different for each person. The following list describes the most common symptoms:
- Leg weakness, including difficulty walking
- Loss of coordination
- Difficulty speaking and swallowing
- Foot deformities
- Foot ulcers
- Hearing loss and/or vision loss
- Eye movement abnormalities
- Movement disorders such as tremor, dystonia, and chorea
Your doctor will ask about your symptoms. You will also be asked about your medical history, family history, and current medication. A physical exam will be done. If Friedrich's ataxia is suspected, you may also see a doctor who specializes in the nervous system.
Images may need to be taken of your bodily structures. This can be done with:
The function of your muscles and nerves may be tested. This can be done with:
The electrical activity of your heart may be assessed. This can be done with:
Your bodily fluids and tissues may be tested. This can be done with:
- Genetic testing for the frataxin gene
- Blood and urine tests
- Nerve or muscle biopsy
There is no known cure for this condition.
Long-term management is aimed at maintaining as much function as possible and controlling symptoms. Some treatments that may help include:
There is no known way to prevent this condition.
- Rimas Lukas, MD
- Reviewed: 03/2014
- Updated: 05/07/2014
All EBSCO Publishing proprietary, consumer health and medical information found on this site is accredited by URAC. URAC's Health Web Site Accreditation Program requires compliance with 53 rigorous standards of quality and accountability, verified by independent audits. To send comments or feedback to our Editorial Team regarding the content please email us at HLEditorialTeam@ebscohost.com.
This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.