
Friedreich's ataxia - Wikipedia
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, peripheral …
Friedreich Ataxia - National Institute of Neurological Disorders and Stroke
Mar 13, 2026 · 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 with walking and …
Friedreich’s Ataxia: Causes, Symptoms & Treatment
Jun 2, 2025 · What Is Friedreich’s Ataxia? Friedreich's ataxia (FA or FRDA) is a rare genetic condition that causes progressive nervous system damage. It may impact your heart function over time. It …
Friedreich's Ataxia - Johns Hopkins Medicine
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 due to nerve injury.
Friedreich Ataxia - National Ataxia Foundation
Learn about Friedreich’s Ataxia (FA), a rare neurodegenerative disorder. Explore symptoms, genetics, and current research initiatives.
Friedreich's ataxia - Harvard Health
Jun 13, 2025 · Friedreich's ataxia is an inherited (genetic) neurological disorder that causes certain nerve cells to deteriorate over time. In many cases this disorder also affects the heart, certain bones, …
Friedreich ataxia: MedlinePlus Genetics
Jul 2, 2021 · Friedreich ataxia is a genetic condition that affects the nervous system and causes movement problems. People with this condition develop impaired muscle coordination (ataxia) that …
Friedreich ataxia | About the Disease | GARD - Genetic and Rare ...
Friedreich ataxia is a genetic condition that affects the nervous system and causes movement problems. People with this condition develop impaired muscle coordination (ataxia) that worsens over time.
Friedreich's Ataxia - Children's Hospital of Philadelphia
Friedreich's ataxia (FA) is a rare, progressive neurogenetic condition found in approximately 1 in 50,000 people worldwide. While FA is relatively rare, it is the most common form of inherited ataxia in children.
Topic 1.5. Early diagnosis of Friedreich ataxia
These Guidelines are intended to assist qualified healthcare professionals make informed treatment decisions about the care of individuals with Friedreich ataxia. They are not intended as a sole source …