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Related websites
Friedreich Ataxia - National Institute of Neurological Disorders and Stroke
WEBfriedreich 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.
Ninds.nih.govFriedreich Ataxia - StatPearls - NCBI Bookshelf
WEBDec 6, 2020 · friedreich ataxia (FA) is the most common hereditary ataxia accounting for approximately 50% of all ataxia cases. It was first reported in 1863 by the German physician Nikolaus Friedreich. The disease causes neurodegeneration and manifests as a combination of difficulty in ambulation, muscle weakness, loss of sensation and …
Ncbi.nlm.nih.govFriedreich Ataxia - GeneReviews® - NCBI Bookshelf
WEBDec 18, 1998 · friedreich ataxia (FRDA) is characterized by slowly progressive ataxia with onset usually before age 25 years (mean age at onset: 10-15 yrs). FRDA is typically associated with dysarthria, muscle weakness, spasticity particularly in the lower limbs, scoliosis, bladder dysfunction, absent lower-limb reflexes, and loss of position and …
Ncbi.nlm.nih.govFriedreich's Ataxia (FA): What It Is, Symptoms & Treatment
WEBFriedreich’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.
My.clevelandclinic.orgClinical management guidelines for Friedreich ataxia: best …
WEBNov 12, 2022 · Individuals with friedreich ataxia (FRDA) can find it difficult to access specialized clinical care. To facilitate best practice in delivering healthcare for FRDA, clinical management guidelines (CMGs) were developed in 2014.
Ncbi.nlm.nih.govFriedreich's Ataxia - Johns Hopkins Medicine
WEBFriedreich'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.
Hopkinsmedicine.orgFriedreich's ataxia - Wikipedia
WEBFriedreich'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 …
En.wikipedia.orgFriedreich ataxia - The BMJ
WEBDec 3, 2013 · Practice A Patient’s Journey. friedreich ataxia. BMJ 2013 ; 347 doi: https://doi.org/10.1136/bmj.f7062 (Published 03 December 2013) Cite this as: BMJ 2013;347:f7062. Article. Related content. Metrics. Responses. Peter Gibilisco, research fellow, patient 1, Adam P Vogel, senior research fellow 2. Author affiliations.
Bmj.comOrphanet: Friedreich ataxia
WEBfriedreich ataxia (FRDA) is an inherited neurodegenerative disorder classically characterized by progressive gait and limb ataxia, dysarthria, dysphagia, oculomotor dysfunction, loss of deep tendon reflexes, pyramidal tract signs, scoliosis, and in some, cardiomyopathy, diabetes mellitus, visual loss and defective hearing. ORPHA:95.
Orpha.netFriedreich's Ataxia - Symptoms, Causes, Treatment | NORD
WEBOct 24, 2023 · Friedreich’s ataxia (FRDA) is a genetic, progressive, neurodegenerative movement disorder, with a typical age of onset between 10 and 15 years. Initial symptoms may include unsteady posture, frequent falling, fatigue and progressive difficulty walking due to impaired ability to coordinate voluntary movements (ataxia).
Rarediseases.org