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Results 1 - 10 of 14 for Ocular dyssynergia
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  1. Ataxia with oculomotor apraxia 
    ... onset ataxia with oculomotor apraxia EAOH Early-onset ataxia with ocular motor apraxia and hypoalbuminemia SCAN2 SCAR1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia, recessive, ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  2. SETX gene 
    ... of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nat Genet. 2004 Mar;36(3):225-7. doi: 10.1038/ng1303. Epub 2004 Feb 8. Citation on PubMed ... ataxia with neuropathy and elevated serum alpha-fetoprotein. Orphanet ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  3. APTX gene 
    ... Makifuchi T, Onodera O. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1. Adv Exp Med Biol. ...
    https://medlineplus.gov/genetics/gene/aptx - Genetics
  4. Eye Movement Disorders (National Library of Medicine)  
    When you look at an object, you're using several muscles to move both eyes to focus on it. If you have a problem with the muscles, the eyes don't work properly. ...
    https://medlineplus.gov/eyemovementdisorders.html - Health Topics
  5. Serotonin syndrome 
    ... signs or symptoms: Agitation Abnormal eye movements called 'ocular ... (ataxia) Serotonin syndrome is not diagnosed until all other ...
    https://medlineplus.gov/ency/article/007272.htm - Medical Encyclopedia
  6. Joubert syndrome 
    ... in infancy, which contributes to difficulty coordinating movements (ataxia) ... (ocular motor apraxia). Most affected individuals have delayed development ...
    https://medlineplus.gov/genetics/condition/joubert-syndrome - Genetics
  7. SRD5A3-congenital disorder of glycosylation 
    ... Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5alpha-Reductase Type 3 Congenital ... de Brouwer AP, Lefeber DJ. A novel cerebello-ocular syndrome with abnormal glycosylation due to abnormalities in ...
    https://medlineplus.gov/...d5a3-congenital-disorder-of-glycosylation - Genetics
  8. Congenital cataracts, facial dysmorphism, and neuropathy 
    ... Walter MC, Lochmuller H, Gooding R, Kalaydjieva L. Ocular features of the congenital cataracts facial dysmorphism neuropathy ...
    https://medlineplus.gov/...taracts-facial-dysmorphism-and-neuropathy - Genetics
  9. Andermann syndrome 
    ... atypical physical features such as widely spaced eyes (ocular hypertelorism); a wide, short skull (brachycephaly); a high ... N, Bouchard JP, Brais B, Rouleau GA. Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian ...
    https://medlineplus.gov/genetics/condition/andermann-syndrome - Genetics
  10. Tyrosinemia 
    ... Rootman D. Tyrosinemia type II: nine cases of ocular signs and symptoms. Am J Ophthalmol. 2001 Oct; ...
    https://medlineplus.gov/genetics/condition/tyrosinemia - Genetics
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