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Friedreich’s ataxia (also called FA or FDRA) is a rare genetic condition that causes progressive nervous system damage and movement issues. It usually begins in childhood and leads to impaired muscle coordination (ataxia) that becomes worse over time. It’s a degenerative disease.
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 nerves, and cerebellum, leading to impaired muscle coordination . The condition typically manifests in childhood or adolescence, with initial ...
Jul 19, 2024 · 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 gait. In FA, nerve fibers in the spinal cord and peripheral nerves break down, becoming thinner.
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.
Dec 6, 2020 · Friedreich ataxia is an inherited disease affecting the nervous system, which produces progressive ataxia, weakness, and sensory deficits. It is inherited as an autosomal recessive disease.
Jan 18, 2024 · Friedreich’s ataxia is a rare genetic disease that causes difficulty walking, a loss of sensation in the arms and legs, and impaired speech. It’s also known as spinocerebellar degeneration ...
Friedreich’s ataxia (FA) is a hereditary neurological degenerative disease characterized by spinocerebellar degeneration (a disease of the tracts going from the cerebellum to the spinal cord).
