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Results 1 - 6 of 6 for Autosomal recessive spinocerebellar ataxia 15
  1. Ataxia with oculomotor apraxia 
    ... with oculomotor apraxia and hypoalbuminemia Genetic Testing Registry: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 Ataxia-oculomotor apraxia 3 ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  2. Infantile-onset spinocerebellar ataxia 
    ... Spelbrink JN, Lonnqvist T, Peltonen L. Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky. Hum Mol Genet. 2005 Oct 15;14(20):2981-90. doi: 10.1093/hmg/ ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  3. TWNK gene 
    ... Spelbrink JN, Lonnqvist T, Peltonen L. Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky. Hum Mol Genet. 2005 Oct 15;14(20):2981-90. doi: 10.1093/hmg/ ...
    https://medlineplus.gov/genetics/gene/twnk - Genetics
  4. Friedreich ataxia 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition. FA FRDA Friedreich spinocerebellar ataxia Friedrich's ataxia Genetic Testing Registry: Friedreich ataxia ...
    https://medlineplus.gov/genetics/condition/friedreich-ataxia - Genetics
  5. Huntington's disease-like syndrome 
    ... disorder. The parents of an individual with an autosomal recessive condition each carry one copy of the altered gene, ... National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../huntingtons-disease-like-syndrome - Genetics
  6. Friedreich ataxia 
    ... faster it gets worse. Friedreich ataxia is an autosomal recessive genetic disorder. This means you must get a ...
    https://medlineplus.gov/ency/article/001411.htm - Medical Encyclopedia