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Results 1 - 10 of 24 for Spinocerebellar ataxia type 2
  1. Spinocerebellar ataxia type 2 
    Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition initially experience ... s mother (maternal inheritance). SCA2 Genetic Testing Registry: Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 2 National Organization for Rare ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  2. Spinocerebellar Ataxias Including Machado-Joseph Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Spinocerebellar ...
    https://www.ninds.nih.gov/...taxias-including-machado-joseph-disease - External Health Links
  3. Ataxia with oculomotor apraxia 
    ... hypoalbuminemia SCAN2 SCAR1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia, recessive, non-Friedreich type 1 Genetic Testing Registry: ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  4. ATXN2 gene 
    ... is repeated approximately 22 times within the gene. Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems ... Gotay D, Jorge Cedeno H. Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in ...
    https://medlineplus.gov/genetics/gene/atxn2 - Genetics
  5. Cerebellar Disorders (National Library of Medicine)  
    When you play the piano or hit a tennis ball you are activating the cerebellum. The cerebellum is the area of the brain that controls coordination and balance. ...
    https://medlineplus.gov/cerebellardisorders.html - Health Topics
  6. Movement Disorders (National Library of Medicine)  
    Movement disorders are neurologic conditions that cause problems with movement, such as: Increased movement that can be voluntary (intentional) or involuntary ( ...
    https://medlineplus.gov/movementdisorders.html - Health Topics
  7. Spinocerebellar ataxia type 1 
    ... BP, Bauer P, Schols L. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6. Mov Disord. 2008 Nov 15; ... P. Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1. Cerebellum. 2008;7(2):106-14. doi: 10.1007/s12311-008-0009- ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  8. ITPR1 gene 
    ... indicate that ITPR1 gene mutations that cause the spinocerebellar ataxias affect different regions of the protein than do ... and symptoms among Gillespie syndrome and the various spinocerebellar ataxias. IP3R IP3R1 Tests of ITPR1 PubMed SPINOCEREBELLAR ATAXIA ...
    https://medlineplus.gov/genetics/gene/itpr1 - Genetics
  9. Huntington's disease-like 
    ... Registry: Huntington disease-like 2 Genetic Testing Registry: Spinocerebellar ataxia type 17 Huntington disease-like 2 National Organization for Rare Disorders (NORD) HUNTINGTON DISEASE- ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease-like - Genetics
  10. Spinocerebellar ataxia type 36 
    ... doi: 10.1002/mds.25092. Epub 2012 Jul 2. Citation on PubMed
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
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