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Results 11 - 14 of 14 for spinocerebellar disease
  1. Autosomal recessive cerebellar ataxia type 1 
    ... National Organization for Rare Disorders (NORD) ... ataxia with SYNE1 mutation accompanying motor neuron disease. Neurology. 2013 Feb 5;80(6):600-1. ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  2. Ataxia with oculomotor apraxia 
    ... raise a person's risk of developing heart disease.Ataxia with oculomotor apraxia type 2 ... SCAR1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia, ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  3. ATXN3 gene 
    ... regulating the first stage of protein production (transcription). ... I. Caring for Machado-Joseph disease: current understanding and how to help patients. Parkinsonism ...
    https://medlineplus.gov/genetics/gene/atxn3 - Genetics
  4. 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
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