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1,924 Possible Causes for Spinocerebellar Ataxia

  • Spinous Process Fracture

    ataxia 18 607458 Disease ID 9976 at NIH's Office of Rare Diseases Spinocerebellar ataxia 19 607346 Disease ID 9969 at NIH's Office of Rare Diseases Spinocerebellar ataxia[en.wikipedia.org] Homepage Rare diseases Search Search for a rare disease Spinocerebellar ataxia type 40 Disease definition Spinocerebellar ataxia type 40 (SCA40) is a very rare subtype of[orpha.net] Wadia (1925-2016) to neurology, in particular, the first description of spinocerebellar ataxia type 2.[scielo.br]

  • Olivopontocerebellar Atrophy

    Spinocerebellar ataxia type 6 (SCA6) is an autosomal dominant, slowly progressive cerebellar ataxia without multisystem involvement.[ncbi.nlm.nih.gov] OPCA is present in several neurodegenerative syndromes, including inherited and non-inherited forms of ataxia (such as the hereditary spinocerebellar ataxia known as Machado-Joseph[ninds.nih.gov] OPCA is present in several neurodegenerative syndromes, including inherited and non-inherited forms of ataxia (such as the hereditary spinocerebellar ataxia known as Machado–Joseph[en.wikipedia.org]

  • Parkinson's Disease Type 3

    Motor cortical dysfunction develops in spinocerebellar ataxia type 3.[frontiersin.org] @article{GwinnHardy2001SpinocerebellarAT, title {Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family.}, author {Katrina A.[semanticscholar.org] Background Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3 (SCA3), can present with parkinsonism.[jamanetwork.com]

  • Ataxia

    What is Spinocerebellar Ataxia?[mda.org.nz] Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia. Am J Med Genet 2000; 95:351.[verywellhealth.com] Campellone, Validating an Ataxia Functional Composite Scale in spinocerebellar ataxia, Journal of the Neurological Sciences, 268, 1-2, (136), (2008).[doi.org]

  • Machado-Joseph Disease

    Homozygosity enhances severity in spinocerebellar ataxia type 3.[ncbi.nlm.nih.gov] Author information 1 Department of Neurosciences, Universitat Autònoma de Barcelona, Barcelona, Spain. amatilla@igtp.cat Abstract The spinocerebellar ataxias (SCAs) are a[ncbi.nlm.nih.gov] Spinocerebellar ataxia type 3 Anelyssa D'Abreu MD (Dr.[medlink.com]

  • Spinocerebellar Ataxia Type 13

    Spinocerebellar Ataxia: Making an Informed Choice about Genetic Testing Booklet providing information about Spinocerebellar Ataxia Ataxia UK Lincoln House 1-3 Brixton Road[ncbi.nlm.nih.gov] spinocerebellar ataxia type 13 Human disease SPINOCEREBELLAR ATAXIA 13 Spinocerebellar Ataxia type 13 SCA13 SPINOCEREBELLAR ATAXIA 13; SCA13 Statements Identifiers Sitelinks[wikidata.org] Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13).[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 6

    Molecular epidemiology of spinocerebellar ataxia type 6.[ncbi.nlm.nih.gov] Spinocerebellar Ataxia is often misdiagnosed as other diseases such as ALC or Parkinson's Disease. There is no known prevention of spinocerebellar ataxia.[en.wikipedia.org] From Wikidata Jump to navigation Jump to search Human disease SCA6 Spinocerebellar Ataxia type 6 SPINOCEREBELLAR ATAXIA 6; SCA6 Spinocerebellar ataxia 6 edit English spinocerebellar[wikidata.org]

  • Neurodegenerative Disorder

    BACKGROUND: Autosomal dominant spinocerebellar ataxias (SCA) are a group of inherited neurodegenerative disorders that typically show peripheral neuropathy.[ncbi.nlm.nih.gov] Spinocerebellar ataxias (SCAs) are dominantly inherited neurodegenerative disorders characterized by progressive cerebellar ataxia and dysarthria.[ncbi.nlm.nih.gov] Abstract Spinocerebellar ataxia type 1 (SCA1) is one of a group of dominantly inherited neurodegenerative diseases caused by a mutant expansion of a polyglutamine-repeated[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 1

    Spinocerebellar ataxia type 1 is an autosomal dominant genetic disease in which progressive central nervous system degeneration (primarily of the cerebellum) results in the[symptoma.com] spinocerebellar ataxia including SCA1 is required.[ncbi.nlm.nih.gov] Spinal cord atrophy in spinocerebellar ataxia type 1.[ncbi.nlm.nih.gov]

  • Boucher-Neuhäuser Syndrome

    A family is described in which two brothers have spinocerebellar ataxia, hypogonadotropic hypogonadism and chorioretinal dystrophy.[ncbi.nlm.nih.gov] Other forms of spinocerebellar ataxia, such as the following: Machado-Joseph Disease : Form of autosomal dominant inherited spinocerebellar ataxia with clinical onset usually[accessanesthesiology.mhmedical.com] OMIM : 57 Boucher-Neuhauser syndrome is an autosomal recessive disorder characterized classically by the triad of spinocerebellar ataxia, hypogonadotropic hypogonadism, and[malacards.org]

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