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Results 1 - 5 of 5 for Autosomal recessive spinocerebellar ataxia 2
  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 Ataxia-oculomotor apraxia type ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  2. Primary coenzyme Q10 deficiency 
    ... PDSS1 PDSS2 This condition is inherited in an autosomal recessive pattern, which means both copies of a gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  3. Myoclonic epilepsy myopathy sensory ataxia 
    ... MEMSA. POLG This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/...yoclonic-epilepsy-myopathy-sensory-ataxia - Genetics
  4. Friedreich ataxia 
    ... ataxia. FXN This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/genetics/condition/friedreich-ataxia - Genetics
  5. Huntington's disease-like 
    ... the gene. HDL3 is probably inherited in an autosomal recessive pattern, which means both copies of the gene ... disorder. The parents of an individual with an autosomal recessive condition each carry one copy of the altered ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease-like - Genetics