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Results 1 - 8 of 8 for Spinocerebellar ataxia type 5
  1. Spinocerebellar ataxia type 2 
    ... Gotay D, Jorge Cedeno H. Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  2. Spinocerebellar ataxia type 3 
    ... Joseph disease. Neurol India. 2009 Sep-Oct;57(5):578-83. doi: 10.4103/0028-3886.57803. Citation on PubMed
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  3. Infantile-onset spinocerebellar ataxia 
    ... Testing Registry: Infantile onset spinocerebellar ataxia ... Finsterer J. Mitochondrial ataxias. Can J Neurol Sci. 2009 Sep;36(5):543-53. doi: 10.1017/s0317167100008027. Citation on ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  4. Spinocerebellar ataxia type 36 
    ... and genetic characterization. Brain. 2012 May;135(Pt 5):1423-35. doi: ... a type of spinocerebellar ataxia accompanied by motor neuron involvement. ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  5. Autosomal recessive cerebellar ataxia type 1 
    ... National Organization for Rare Disorders (NORD) ... recessive cerebellar ataxia. Nat Genet. 2007 Jan;39(1):80-5. doi: 10.1038/ng1927. Epub 2006 Dec 10. ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  6. Huntington's disease-like syndrome 
    ... disease-like 2 Genetic Testing Registry: Spinocerebellar ataxia type 17 ... genetically heterogeneous. Mov Disord. 2008 Apr 15;23(5):716-20. doi: 10.1002/mds.21915. Citation ...
    https://medlineplus.gov/.../huntingtons-disease-like-syndrome - Genetics
  7. Ataxia with oculomotor apraxia 
    ... EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH SPINOCEREBELLAR ... with oculomotor apraxia type 4. Am J Hum Genet. 2015 Mar 5;96(3):474-9. doi: 10.1016/j. ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  8. Primary coenzyme Q10 deficiency 
    Primary coenzyme Q10 deficiency is a disorder that can affect many parts of the body, especially the brain, muscles, and kidneys. As its name suggests, the disorder ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics