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Results 1 - 6 of 6 for Limb dysmetria
  1. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN) is a nervous system disorder with signs and symptoms that usually begin in mid-adulthood ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  2. Ataxia with oculomotor apraxia 
    ... XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia. Nature. 2017 Jan 5;541(7635):87-91. ... Beis JM, Brice A, Koenig M, Durr A. Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  3. Autosomal recessive spastic ataxia of Charlevoix-Saguenay 
    ... the muscles (spasticity), problems with balance and coordination (cerebellar ataxia), and reduced sensation and weakness in the arms ... Autosomal recessive spastic ataxia of Charlevoix-Saguenay: upper extremity aptitudes, functional independence and social participation. Int J ...
    https://medlineplus.gov/...ive-spastic-ataxia-of-charlevoix-saguenay - Genetics
  4. Myoclonic epilepsy with ragged-red fibers 
    ... Kay CK, Raskin S, Werneck LC, Bruhn H. Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report. ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  5. Alpha-methylacyl-CoA racemase deficiency 
    ... PF. AMACR mutations cause late-onset autosomal recessive cerebellar ataxia. Neurology. 2011 May 17;76(20):1768-70. ...
    https://medlineplus.gov/.../alpha-methylacyl-coa-racemase-deficiency - Genetics
  6. AMACR gene 
    ... PF. AMACR mutations cause late-onset autosomal recessive cerebellar ataxia. Neurology. 2011 May 17;76(20):1768-70. ...
    https://medlineplus.gov/genetics/gene/amacr - Genetics