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Friedreich Ataxia
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Friedreich Ataxia Learning Center
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Friedreich Ataxia
Friedreich's ataxia (FRDA) is a rare inherited disease. The two main features of this disorder are: progressive loss of voluntary muscular coordination (ataxia) heart enlargement Diagnosis is usually made between ages 8...
Basic Info
Symptoms
Symptoms are caused by the wearing away of structures in areas of the brain and spinal cord that control coordination, ...
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Causes
Friedreich's ataxia is caused by a defect in a gene called Frataxin (FXN), which is located on chromosome 9. Changes in...
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Tests
The following tests may be performed: ECG; Genetic testing for the frataxin gene; X-ray of the chest; X-ray of the spin...
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Treatments
Treatment for Friedreich's ataxia includes: Counseling; Speech therapy; Physical therapy; Walking aids or wheelchairs. ...
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Supplements
Safflower
Safflower Oil
ubiquinone
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Complications
Loss of ability to move around; Heart failure or heart disease; Diabetes.
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Prevention
Individuals with a family history of Friedreich's ataxia who intend to have children should consider genetic screening ...
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Doctor Specialties
Call your health care provider if muscle weakness, numbness, loss of coordination, loss of reflexes, or other symptoms ...
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Basic Info
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UCLA Seeks Patients 8-to-17 with F...
MitoSciences Inc. Releases New Tes...
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Central nervous system and periphe...
Friedreich ataxia, on chromosome ...
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