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Results 1 - 10 of 12 for Spinocerebellar ataxia type 20
  1. Spinocerebellar ataxia type 1 
    ... Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1. J Biol Chem. 2009 Mar 20;284(12):7425-9. doi: 10.1074/jbc. ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  2. ATXN1 gene 
    ... Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1. J Biol Chem. 2009 Mar 20;284(12):7425-9. doi: 10.1074/jbc. ...
    https://medlineplus.gov/genetics/gene/atxn1 - Genetics
  3. Spinocerebellar ataxia type 3 
    ... require wheelchair assistance. They usually survive 10 to 20 years after symptoms first appear. The prevalence of SCA3 is unknown. This condition is thought to be the most common type of spinocerebellar ataxia; however, all types of spinocerebellar ataxia are relatively ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  4. Spinocerebellar ataxia type 2 
    ... adulthood. People with SCA2 usually survive 10 to 20 years after symptoms first appear. The prevalence of SCA2 is unknown. This condition is estimated to be one of the most common types of spinocerebellar ataxia; however, all types of spinocerebellar ataxia are relatively ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  5. Spinocerebellar Ataxias Including Machado-Joseph Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    From the National Institutes of Health ... Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... Spinocerebellar ...
    https://www.ninds.nih.gov/...taxias-including-machado-joseph-disease - External Health Links
  6. CACNA1A gene 
    ... swelling and coma. More About This Health Condition Spinocerebellar ... the number of CAG repeats ranges from 20 to more than 30.An increase in the ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  7. Infantile-onset spinocerebellar ataxia 
    ... Disorders (NORD) MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL ... 20. Citation on PubMed Lonnqvist T. Infantile-Onset Spinocerebellar ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  8. TWNK gene 
    ... TWNK PubMed MITOCHONDRIAL DNA DEPLETION SYNDROME 3 ... ataxia and mitochondrial recessive ataxia syndrome are associated with ...
    https://medlineplus.gov/genetics/gene/twnk - Genetics
  9. Ataxia with oculomotor apraxia 
    ... EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH SPINOCEREBELLAR ... Epub 2009 Aug 20. Citation on PubMed Bras J, Alonso I, Barbot ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  10. Spinocerebellar ataxia type 6 
    Spinocerebellar ataxia type 6 ... People with 20 repeats tend to experience signs and symptoms of SCA6 beginning ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
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