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Results 31 - 40 of 40 for Ocular motility disease
  1. RNAse T2-deficient leukoencephalopathy 
    ... hands (athetosis), uncontrolled muscle tensing (dystonia), and involuntary eye movements (nystagmus). In addition to the neurological problems associated ...
    https://medlineplus.gov/.../rnase-t2-deficient-leukoencephalopathy - Genetics
  2. Multiple system atrophy 
    ... also include speech difficulties (dysarthria) and problems controlling eye movement.Multiple system atrophy usually occurs in older adults; ... It is unclear whether these variations also affect disease risk in other populations. The COQ2 gene provides ...
    https://medlineplus.gov/genetics/condition/multiple-system-atrophy - Genetics
  3. Ocular albinism 
    ... abnormalities associated with this condition include rapid, involuntary eye movements (nystagmus); eyes that do not look in the ... OA XLOA Genetic Testing Registry: Aland island eye disease Genetic Testing Registry: Ocular albinism with late-onset ...
    https://medlineplus.gov/genetics/condition/ocular-albinism - Genetics
  4. Oculopharyngeal muscular dystrophy 
    ... to impair vision, and in some cases, limit eye movement. Along with ptosis, affected individuals develop weakness of ... CORNEMUS and FILNEMUS. Correlation between PABPN1 genotype and disease severity in oculopharyngeal muscular dystrophy. Neurology. 2017 Jan ...
    https://medlineplus.gov/.../oculopharyngeal-muscular-dystrophy - Genetics
  5. X-linked sideroblastic anemia and ataxia 
    ... dysdiadochokinesis). Mild speech difficulties (dysarthria), tremor, and abnormal eye movements have also been reported in some affected individuals. ... X-linked sideroblastic anaemia with ataxia: another mitochondrial disease? J Neurol Neurosurg Psychiatry. 2001 Jan;70(1): ...
    https://medlineplus.gov/.../x-linked-sideroblastic-anemia-and-ataxia - Genetics
  6. Myasthenia gravis 
    ... drooping of the eyelids (ptosis) and difficulty coordinating eye movements, which results in blurred or double vision. In ... of developing other autoimmune disorders, including autoimmune thyroid disease and systemic lupus erythematosus. Gene variations that affect ...
    https://medlineplus.gov/genetics/condition/myasthenia-gravis - Genetics
  7. Triosephosphate isomerase deficiency 
    ... of the skin and the whites of the eyes.Movement problems typically become apparent by age 2 in ... Triosephosphate isomerase deficiency: new insights into an enigmatic disease. Biochim Biophys Acta. 2009 Dec;1792(12):1168- ...
    https://medlineplus.gov/.../triosephosphate-isomerase-deficiency - Genetics
  8. Autosomal recessive cerebellar ataxia type 1 
    ... scale (dysmetria). Other features of ARCA1 include abnormal eye movements (nystagmus) and problems following the movements of objects ... Cerebellar 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
  9. Lissencephaly with cerebellar hypoplasia 
    ... life. Some affected individuals have nearsightedness (myopia), involuntary eye movements (nystagmus), or puffiness or swelling caused by a ... The role of RELN in lissencephaly and neuropsychiatric disease. Am J Med Genet B Neuropsychiatr Genet. 2007 ...
    https://medlineplus.gov/.../lissencephaly-with-cerebellar-hypoplasia - Genetics
  10. Color vision deficiency 
    ... sensitivity to light (photophobia), involuntary back-and-forth eye movements (nystagmus), and nearsightedness (myopia). Blue cone monochromacy is ... be caused by other eye disorders, such as diseases involving the retina, the nerve that carries visual ...
    https://medlineplus.gov/genetics/condition/color-vision-deficiency - Genetics
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