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Results 21 - 30 of 40 for Ocular motility disease
  1. Abetalipoproteinemia 
    ... may also have other eye problems, including involuntary eye movements (nystagmus), eyes that do not look in the ... neuropathy ABL Acanthocytosis Apolipoprotein B deficiency Bassen-Kornzweig disease Bassen-Kornzweig syndrome Betalipoprotein deficiency disease Congenital betalipoprotein ...
    https://medlineplus.gov/genetics/condition/abetalipoproteinemia - Genetics
  2. Cone-rod dystrophy 
    ... As the condition progresses, individuals may develop involuntary eye movements (nystagmus).There are more than 30 types of ... rod dystrophy are also associated with other eye diseases, including a group of related eye disorders called ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  3. Kallmann syndrome 
    ... roof of the mouth (a cleft palate), abnormal eye movements, hearing loss, and abnormalities of tooth development. Some ... Kallmann syndrome, but are unlikely to cause the disease on their own.The genes associated with Kallmann ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  4. Leigh syndrome 
    ... muscles that move the eyes (ophthalmoparesis); rapid, involuntary eye movements (nystagmus); or degeneration of the nerves that carry ... subacute necrotizing encephalopathy Juvenile subacute necrotizing encephalopathy Leigh disease Leigh's disease Subacute necrotizing encephalomyelopathy Genetic Testing ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  5. GLUT1 deficiency syndrome 
    ... first sign of the disorder may be involuntary eye movements that are rapid and irregular. Babies with common ... signs and symptoms of the condition. De Vivo disease Encephalopathy due to GLUT1 deficiency G1D Glucose transport ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
  6. Dopamine transporter deficiency syndrome 
    ... signs and symptoms that can develop include abnormal eye movements; reduced facial expression (hypomimia); disturbed sleep; frequent episodes ... transporter deficiency syndrome appears to be a rare disease; only about 20 affected individuals have been described ...
    https://medlineplus.gov/.../dopamine-transporter-deficiency-syndrome - Genetics
  7. Congenital cataracts, facial dysmorphism, and neuropathy 
    ... small or poorly developed eyes (microphthalmia) and abnormal eye movements (nystagmus). Affected individuals, particularly males, often have distinctive ...
    https://medlineplus.gov/...taracts-facial-dysmorphism-and-neuropathy - Genetics
  8. Achromatopsia 
    ... light and glare (photophobia), involuntary back-and-forth eye movements (nystagmus), and significantly reduced sharpness of vision (low ... S, van Genderen MM, Riemslag FC; European Retinal Disease Consortium; Lukowski R, den Hollander AI, Cremers FP, ...
    https://medlineplus.gov/genetics/condition/achromatopsia - Genetics
  9. X-linked myotubular myopathy 
    ... also have weakness in the muscles that control eye movement (ophthalmoplegia), weakness in other muscles of the face, ... recurrent ear and respiratory infections, seizures, or liver disease. Some affected individuals develop a serious liver condition ...
    https://medlineplus.gov/.../condition/x-linked-myotubular-myopathy - Genetics
  10. Neuroblastoma 
    ... may develop opsoclonus myoclonus syndrome, which causes rapid eye movements and jerky muscle motions. This condition occurs when ... neuroblastoma is associated with the severity of the disease but not thought to cause it. About 25 ...
    https://medlineplus.gov/genetics/condition/neuroblastoma - Genetics
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