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Results 1 - 10 of 52 for Ocular motility disease
  1. Progressive supranuclear palsy 
    ... vertical gaze palsy) is a hallmark of this disease. Other eye movement problems include difficulty opening and closing the eyelids, ...
    https://medlineplus.gov/.../condition/progressive-supranuclear-palsy - Genetics
  2. Gaucher disease 
    ... symptoms described above, these conditions can cause abnormal eye movements, seizures, and brain damage. Type 2 Gaucher disease usually causes life-threatening medical problems beginning in ...
    https://medlineplus.gov/genetics/condition/gaucher-disease - Genetics
  3. Deoxyguanosine kinase deficiency 
    ... may include weak muscle tone (hypotonia), abnormal involuntary eye movements (nystagmus), developmental delays, and, rarely, seizures. Early signs of liver disease may include an enlarged liver (hepatomegaly) and yellowing ...
    https://medlineplus.gov/.../deoxyguanosine-kinase-deficiency - Genetics
  4. PLP1 gene 
    ... that primarily affects males. Individuals with Pelizaeus-Merzbacher disease have neurological problems including abnormal eye movements (nystagmus) and other movement abnormalities. In addition, these ...
    https://medlineplus.gov/genetics/gene/plp1 - Genetics
  5. Wilson disease 
    ... the colored part of the eye. Abnormalities in eye movements, such as a restricted ability to gaze upwards, may also occur. Wilson disease is a rare disorder that affects approximately 1 ...
    https://medlineplus.gov/genetics/condition/wilson-disease - Genetics
  6. CLN11 disease 
    ... lenses of the eyes (cataracts) and rapid, involuntary eye movements ... time, people with CLN11 disease develop short-term memory loss and loss of ...
    https://medlineplus.gov/genetics/condition/cln11-disease - Genetics
  7. Frontotemporal dementia with parkinsonism-17 
    ... FTDP-17 also have restricted up-and-down eye movement (vertical gaze palsy) and rapid abnormal movements of both eyes (saccades). The worldwide prevalence of FTDP-17 is unknown. In the Netherlands, where the disease prevalence has been studied, it is estimated to ...
    https://medlineplus.gov/...ntotemporal-dementia-with-parkinsonism-17 - Genetics
  8. Mitochondrial neurogastrointestinal encephalopathy disease 
    ... eyelids (ptosis), weakness of the muscles that control eye movement (ophthalmoplegia), and hearing loss. Leukoencephalopathy, which is the deterioration of a type of brain tissue known as white matter, is a hallmark of MNGIE disease. These changes in the brain can be seen ...
    https://medlineplus.gov/...rogastrointestinal-encephalopathy-disease - Genetics
  9. Multiminicore disease 
    ... of multiminicore disease.The ophthalmoplegic form of multiminicore disease is characterized by paralysis of the eye muscles (external ophthalmoplegia). This can lead to abnormal eye movements and droopy eyelids (ptosis). This form of the ...
    https://medlineplus.gov/genetics/condition/multiminicore-disease - Genetics
  10. TPP1 gene 
    ... as involuntary movement of the eyes (nystagmus), rapid eye movements ... with CLN2 disease (described above), individuals with SCAR7 likely have a ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
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