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Results 1 - 10 of 10 for Limb dysmetria
  1. Learning about Fragile X Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Fragile X syndrome is an inherited intellectual disability caused by a mutation in the FMR1 gene. ... Fragile X Syndrome/Start Here ... Fragile X Syndrome ... National ...
    https://www.genome.gov/Genetic-Disorders/Fragile-X-Syndrome - External Health Links
  2. 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
  3. Acute cerebellar ataxia 
    ... Barr, echovirus , among others. Other causes of acute cerebellar ... diseases associated with some cancers (paraneoplastic disorders)
    https://medlineplus.gov/ency/article/001397.htm - Medical Encyclopedia
  4. 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
  5. Progressive Supranuclear Palsy (PSP): Frequently Asked Questions (Foundation for PSP/CBD and Related Brain Diseases)  
    Progressive Supranuclear Palsy/Learn More ... Progressive Supranuclear Palsy ... Foundation for PSP/CBD and Related Brain Diseases
    https://www.psp.org/iwanttolearn/faq - External Health Links
  6. Movement - uncoordinated 
    ... that are passed through families (such as congenital cerebellar ataxia, Friedreich ataxia , ataxia - telangiectasia , or Wilson disease ) Multiple ...
    https://medlineplus.gov/ency/article/003198.htm - Medical Encyclopedia
  7. 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
  8. 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
  9. 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
  10. 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