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1,546 Possible Causes for Friedreich Ataxia

  • Talipes Cavus

    Pes cavus is oftentimes—but not always—connected through Hereditary Motor and Sensory Neuropathy Type 1 (Charcot-Marie-Tooth disease) and Friedreich's Ataxia; many other cases[drfosdick.com] Various other web sites were mentioning pes cavus in realtion to Charcot-Marie-Tooth (CMT) and to Friedreich's ataxia, which come up in many of the HSP papers I've found.[hspjourney.blogspot.com] ataxia, cerebral palsy, and spinal cord tumors, can cause muscle imbalances that lead to elevated arches.[physiotherapy-treatment.com]

  • Ataxia Telangiectasia

    Differential diagnosis of ataxia- telangiectasia Other inherited disorders to consider include: Friedreich ataxia Ataxia-oculomotor apraxia Familial spinocerebellar atrophy[dermnetnz.org] However, Friedreich ataxia usually has a later onset.[encyclopedia.com] Once disease progression becomes apparent, Friedreich ataxia (a degenerative disease of the spinal cord ) becomes the most common misdiagnosis.[encyclopedia.com]

  • Fitzsimmons-McLachlan-Gilbert Syndrome

    ataxia congenital glaucoma Friedreich's ataxia Frigophobia Froelich's syndrome Frölich's syndrome Fronto nasal malformation cloacal exstrophy Frontofacionasal dysplasia type[bioreference.net] ataxia congenital glaucoma Friedreich's ataxia Fro-Fru Froelich's syndrome Frölich's syndrome Fronto nasal malformation cloacal exstrophy Frontofacionasal dysplasia type[wikidoc.org] Maia Pinheiro Opitz syndrome Frenkel Russe syndrome Frey's syndrome Frias syndrome Fried Goldberg Mundel syndrome Friedel Heid Grosshans syndrome Friedman Goodman syndrome Friedreich[bioreference.net]

  • Ataxia

    Treatment for Friedreich’s ataxia There is currently no cure for Friedreich’s ataxia.[betterhealth.vic.gov.au] What is Friedreich’s ataxia? Friedreich's ataxia (also called FA or FRDA) is an inherited disease that causes progressive damage to the nervous system.[christopherreeve.org] ataxia People with Friedreich's ataxia usually need a wheelchair 15 to 20 years after symptoms first appear.[medlineplus.gov]

  • Paramyoclonus Multiplex

    The gene for Friedreich’s ataxia was mapped to chromosome 9 in 1988.[jnnp.bmj.com] Friedreich ataxia - sclerosis of the posterior and lateral columns of the spinal cord, occurring in children and marked by ataxia in the lower extremities, extending to the[medical-dictionary.thefreedictionary.com] Friedreich’s ataxia, a spinocerebellar degeneration, is an autosomal recessive disease of the cerebellum, spinal cord, and peripheral nerves.[jnnp.bmj.com]

  • Generalized Myotonia of Thomsen

    Treatment for Friedreich’s ataxia There is no cure for Friedreich’s ataxia.[betterhealth.vic.gov.au] What is Friedreich’s Ataxia?[mda.org.au] ataxia People with Friedreich's ataxia usually need a wheelchair 15 to 20 years after symptoms first appear.[medlineplus.gov]

  • Oculomotor Apraxia

    Friedreich's ataxia (FRDA) is a rare autosomal recessive spinocerebellar ataxia which in the majority of cases is associated with a GAA-trinucleotide repeat expansion in the[ncbi.nlm.nih.gov] An unusual phenotype of Friedreich ataxia. Neurogenetics 2010;11:261-5. Nieto A, Correia R, de Nóbrega E, Montón F, Hess S, Barroso J. Cognition in Friedreich ataxia.[acta.tums.ac.ir] Friedreich's ataxia (FRDA) and ataxia with oculomotor apraxia type 2 (AOA2) are the two most frequent forms of autosomal recessive cerebellar ataxias.[curefa.org]

  • Parenchymatous Cortical Cerebellar Degeneration

    Summary Epidemiology This group encompasses a large number of rare diseases, the most frequent in the Caucasian population being Friedreich ataxia (estimated prevalence 2-[orpha.net] Similar Codes ICD-9 Code ICD-9 Description 334.0 Friedreich's ataxia 334.1 Hereditary spastic paraplegia 334.2 Primary cerebellar degeneration 334.3 Other cerebellar ataxia[healthprovidersdata.com] , Hereditary, NOS Example: Friedreich ataxia cerebellar, spinal atrophy Can be divided into autosomal dominant, autosomal recessive, X-linked, mitochondrial Some etiologies[neupsykey.com]

  • Autosomal Recessive Spinocerebellar Ataxia 8

    Delatycki MB et al. (2000) Friedreich ataxia: an overview. J Med Genet 37(1): 1-8. Full text on PubMed. 3.[forgottendiseases.org] friedreichs ataxia Cervicothoracic neuromuscular scoliosis due to friedreich's ataxia Cervicothoracic scoliosis due to friedreichs ataxia Early onset cerebellar ataxia Friedreich's[icd10data.com] All the Friedreich’s ataxia patients in the Algerian cohort had mutations in the FXN gene.[friedreichsataxianews.com]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Friedreich ataxia accounts for one-third of the cases in Caucasians; the others are due to a growing list of very rare molecular defects, including mild forms of metabolic[neurology.org] friedreichs ataxia Cervicothoracic neuromuscular scoliosis due to friedreich's ataxia Cervicothoracic scoliosis due to friedreichs ataxia Early onset cerebellar ataxia Friedreich's[icd10data.com] Tags: acute onset cerebellar ataxia , autosomal recessive cerebellar ataxia , cerebellar ataxia , cerebellar dysfunction , Friedreich's ataxia , neurodegenerative diseases[blogs.nejm.org]

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