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Results 1 - 7 of 7 for Spinocerebellar atrophy
  1. Spinocerebellar ataxia type 1 
    ... 40 repeats or more). Olivopontocerebellar atrophy I SCA1 Spinocerebellar atrophy I Type 1 spinocerebellar ataxia Genetic Testing Registry: Spinocerebellar ataxia type 1 ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  2. 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
  3. Spinocerebellar ataxia type 36 
    Spinocerebellar ataxia type 36 ... swallowing liquids. As the condition progresses, individuals with SCA36 develop ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  4. Autosomal recessive cerebellar ataxia type 1 
    ... National Organization for Rare Disorders (NORD) ... Citation on PubMed
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  5. Infantile-onset spinocerebellar ataxia 
    Infantile-onset ... caused by nerve damage (sensorineural hearing loss) typically occurs during ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  6. Boucher-Neuhäuser syndrome 
    ... syndrome, it arises from a loss of cells (atrophy) in the part of the brain involved in ... hypogonadism Spinocerebellar ataxia, hypogonadotropic hypogonadism, ...
    https://medlineplus.gov/.../condition/boucher-neuhauser-syndrome - Genetics
  7. 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