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Results 11 - 20 of 40 for Ocular motility disease
  1. Tyrosine hydroxylase deficiency 
    ... may resemble those seen in people with Parkinson disease: stiffness of the muscles ... and intellectual disabilities. People with TH-deficient infantile ...
    https://medlineplus.gov/.../tyrosine-hydroxylase-deficiency - Genetics
  2. Camurati-Engelmann disease 
    Camurati-Engelmann disease is a skeletal condition that is characterized by abnormally thick bones (hyperostosis) in the arms, legs, and skull.The thick limb bones ...
    https://medlineplus.gov/.../condition/camurati-engelmann-disease - Genetics
  3. Pol III-related leukodystrophy 
    ... Pol III-related leukodystrophy often have abnormalities in eye movement, such as progressive vertical gaze palsy, which is restricted up-and-down eye movement that worsens over time. Nearsightedness is common in ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  4. Spinocerebellar ataxia type 1 
    ... spasticity), and weakness in the muscles that control eye movement (ophthalmoplegia). Eye muscle weakness leads to rapid, involuntary eye movements (nystagmus). Individuals with SCA1 may have difficulty processing, ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  5. Fatty acid hydroxylase-associated neurodegeneration 
    ... nerves) and difficulties with the muscles that control eye movement. Affected individuals may have a loss of sharp ... look in the same direction (strabismus), rapid involuntary eye movements (nystagmus), or difficulty moving the eyes intentionally (supranuclear ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  6. Primary coenzyme Q10 deficiency 
    ... muscle contractions (dystonia), progressive muscle stiffness (spasticity), abnormal eye movements (nystagmus), vision loss caused by degeneration (atrophy) of ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  7. Mitochondrial complex I deficiency 
    ... or kidney problems. Vision problems due to abnormal eye movement or breakdown (degeneration) of the nerves that carry ... These syndromes can also have other causes. Mitochondrial diseases are thought to occur in about 1 in ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  8. Intestinal pseudo-obstruction 
    ... and limbs, weakness in the muscles that control eye movement (ophthalmoplegia), intellectual disability, seizures, unusual facial features, or ... in the intestinal tract, such as Parkinson's disease, type 2 diabetes, various types of muscular dystrophy, ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  9. Infantile neuroaxonal dystrophy 
    ... Seizures occur in some affected children.Rapid, involuntary eye movements (nystagmus), eyes that do not look in the ... as well as the more common Alzheimer's disease and Parkinson's disease, also are associated with ...
    https://medlineplus.gov/.../infantile-neuroaxonal-dystrophy - Genetics
  10. Joubert syndrome 
    ... or slow (apnea) breathing in infancy, and abnormal eye movements (ocular motor apraxia). Most affected individuals have delayed ... split in a structure of the eye), kidney disease (including polycystic kidney disease and nephronophthisis), liver disease, ...
    https://medlineplus.gov/genetics/condition/joubert-syndrome - Genetics
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