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Results 1 - 3 of 3 for Spinocerebellar "ataxia," autosomal recessive 30
  1. 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
  2. Boucher-Neuhäuser syndrome 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy ... hypogonadism Spinocerebellar ataxia, hypogonadotropic hypogonadism, ...
    https://medlineplus.gov/.../condition/boucher-neuhauser-syndrome - Genetics
  3. Friedreich ataxia 
    ... GAA). Normally, the body contains about 8 to 30 copies of GAA. ... autosomal recessive genetic disorder. This means you must get a ...
    https://medlineplus.gov/ency/article/001411.htm - Medical Encyclopedia