2025年3月26日 · Friedreich ataxia (FA) is a rare, inherited disorder that causes progressive damage to the nervous system. This can cause movement and sensory symptoms and trouble …

Friedreich's ataxia (FRDA) is a rare, inherited, autosomal recessive neurodegenerative disorder that primarily affects the nervous system, causing progressive damage to the spinal cord, …

Friedreich’s ataxia (FA) is a rare inherited condition that damages your nervous system. It causes muscle weakness, balance issues and sensory deficits that worsen over time. Symptoms most …

First described by German physician Nikolaus Friedreich in 1863, Friedreich’s ataxia (known as FA or FRDA) is a neuromuscular disease that mainly affects the nervous system and the …

2020年12月6日 · FA is the most common hereditary ataxia, accounting for approximately 50% of all ataxia cases and approximately 75% in patients less than 25 years of age. In the United …

Friedreich’s ataxia (FA) is a genetic, progressive neuromuscular disease. People with FA experience issues with balance and coordination of movement that lead to life-altering loss of …

Friedreich's ataxia is a rare, inherited, degenerative disease that damages the spinal cord, peripheral nerves and the cerebellum. It causes movement problems and loss of sensation …

Friedreich’s Ataxia is an inherited disease of the central nervous system. It was named after Nikolaus Friedreich, who first described it in 1863, and it was the first form of hereditary Ataxia …

2023年1月12日 · Friedreich ataxia (FA) is a genetic disease with an autosomal-recessive inheritance pattern. Symptoms usually start in childhood or early adolescence, mostly in …

Friedreich’s ataxia is a complex disease that affects each person differently. Learn about FA clinical guidelines, assembling a care team, the FDA approved treatment for FA, …