Sponsored diagnostic testing programs for Friedrich Ataxia (FA)
Friedreich ataxia (FA) is an inherited neuromuscular disorder caused by changes in the FXN gene, leading to impaired nerve function and progressive loss of coordination and balance. Symptoms often include gait instability, limb ataxia, sensory neuropathy, and fatigue, with some individuals also developing cardiomyopathy or diabetes. Genetic testing helps confirm the diagnosis, clarify family risk, and distinguish FA from other inherited or acquired ataxias.
1 program found for Friedrich Ataxia (FA)
Sponsored by Biogen, this program offers no-cost genetic testing for Friedreich ataxia (FA) to support diagnosis and evaluation of patients with suspected or confirmed FA. Testing is available for individuals ≥16 years residing in the U.S. or Puerto Rico and must be ordered by a qualified provider.
