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Results 11 - 20 of 41 for Dysmetria
  1. 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
  2. Ataxia-pancytopenia syndrome 
    ... with movements that involve judging distance or scale (dysmetria), uncontrollable muscle contractions (clonus), and involuntary back-and- ... Baranko PV, Potter NU. Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia. ...
    https://medlineplus.gov/.../condition/ataxia-pancytopenia-syndrome - Genetics
  3. Hartnup disease 
    ... which can include skin rashes; difficulty coordinating movements (cerebellar ataxia); and psychiatric symptoms, such as depression or psychosis. ... signs and symptoms of this condition including rashes, cerebellar ataxia, and psychiatric symptoms. Researchers believe that many of ...
    https://medlineplus.gov/genetics/condition/hartnup-disease - Genetics
  4. RNF216 gene 
    ... sexual development (hypogonadotropic hypogonadism) and difficulty coordinating movements (cerebellar ataxia). Many people with Gordon Holmes syndrome caused by ...
    https://medlineplus.gov/genetics/gene/rnf216 - Genetics
  5. GRN gene 
    ... epilepsy), vision loss, problems with balance and coordination (cerebellar ataxia), and a decline in intellectual function that typically ... the brain leads to the development of epilepsy, cerebellar ataxia, and other signs and symptoms in adolescence or ...
    https://medlineplus.gov/genetics/gene/grn - Genetics
  6. Myoclonic epilepsy myopathy sensory ataxia 
    ... SCAE).The first symptom of MEMSA is usually cerebellar ataxia, which refers to problems with coordination and balance ...
    https://medlineplus.gov/...yoclonic-epilepsy-myopathy-sensory-ataxia - Genetics
  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 ...
    https://medlineplus.gov/...ive-spastic-ataxia-of-charlevoix-saguenay - Genetics
  8. ABCB7 gene 
    ... Hellier K, Hammans S, May A. X-linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation ...
    https://medlineplus.gov/genetics/gene/abcb7 - Genetics
  9. Congenital cataracts, facial dysmorphism, and neuropathy 
    ... with movements that involve judging distance or scale (dysmetria). Some have mild intellectual disability. Individuals with CCFDN ...
    https://medlineplus.gov/...taracts-facial-dysmorphism-and-neuropathy - Genetics
  10. SETX gene 
    ... frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein. Orphanet ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
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