The conclusive diagnosis can be made by genetic testing for the FXN gene mutation. An electromyogram (EMG), which measures the

Research on Friedreich’s ataxia syndrome focuses on a variety of topics, including the precise reason for the FXN gene mutation,

The majority of patients start using a wheelchair within 10 to 20 years of the onset of their first symptoms. Those

Your doctor will examine your medical history and do a checkup to determine whether you have Friedreich’s ataxia. To diagnose

Ataxia is usually caused by damage to a part of the brain controlling muscle movement, called the “cerebellum”. It can

Symptoms can develop suddenly or come on progressively over time. The type and onset of symptoms varies with the type

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Ataxia means “the loss of full control of bodily movements”. Ataxia is the term for a group of rare conditions

The first symptom of Friedreich ataxia is usually unsteadiness. Parents may notice that their child falls over or appears to

International Ataxia Awareness Day (IAAD) is on September 25 of each year. It is a coordinated effort from individuals and