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Results 11 - 20 of 31 for Ophthalmoplegia
  1. Mitochondrial DNA 
    ... the eyes, causing weakness of the eye muscles (ophthalmoplegia) and breakdown of the light-sensing tissue at ... involved in an eye condition called progressive external ophthalmoplegia. This disorder weakens the muscles that control eye ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  2. MT-TL1 gene 
    ... cases of an eye condition called progressive external ophthalmoplegia. This disorder weakens the muscles that control eye ... drooping eyelids (ptosis).Some cases of progressive external ophthalmoplegia result from the A3243G mutation, which is the ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  3. Mitochondrial neurogastrointestinal encephalopathy disease 
    ... weakness of the muscles that control eye movement (ophthalmoplegia), and hearing loss. Leukoencephalopathy, which is the deterioration ... the condition. MEPOP ... ophthalmoplegia, and pseudo-obstruction Mitochondrial neurogastrointestinal encephalopathy syndrome MNGIE ...
    https://medlineplus.gov/...rogastrointestinal-encephalopathy-disease - Genetics
  4. OPA1 gene 
    ... Condition MedlinePlus Genetics provides information about Progressive external ophthalmoplegia More About This Health Condition About 20 percent ... the muscles that control eye movement (progressive external ophthalmoplegia), difficulty with balance and coordination (ataxia), disturbances in ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  5. Multiminicore disease 
    ... characterized by paralysis of the eye muscles (external ophthalmoplegia). This can lead to abnormal eye movements and ... Genetic Testing Registry: Congenital multicore myopathy with external ophthalmoplegia Congenital multicore myopathy with external ophthalmoplegia Minicore myopathy, ...
    https://medlineplus.gov/genetics/condition/multiminicore-disease - Genetics
  6. Kearns-Sayre syndrome 
    ... People with Kearns-Sayre syndrome have progressive external ophthalmoplegia, which is weakness or paralysis of the eye ... as ragged-red fibers.A related condition called ophthalmoplegia-plus may be diagnosed if an individual has ...
    https://medlineplus.gov/genetics/condition/kearns-sayre-syndrome - Genetics
  7. Intestinal pseudo-obstruction 
    ... weakness in the muscles that control eye movement (ophthalmoplegia), intellectual disability, seizures, unusual facial features, or recurrent ... NORD) ClinicalTrials.gov ... FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED; CIIPX ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  8. Infantile-onset spinocerebellar ataxia 
    ... weakness in the muscles that control eye movement (ophthalmoplegia). In their teenage years they experience degeneration of ... and symptoms of the condition. IOSCA Ohaha syndrome Ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis Genetic Testing Registry: ...
    https://medlineplus.gov/.../infantile-onset-spinocerebellar-ataxia - Genetics
  9. X-linked myotubular myopathy 
    ... weakness in the muscles that control eye movement (ophthalmoplegia), weakness in other muscles of the face, and ...
    https://medlineplus.gov/.../condition/x-linked-myotubular-myopathy - Genetics
  10. Guillain-Barré syndrome 
    ... paralysis of the muscles that move the eyes (ophthalmoplegia), problems with balance and coordination (ataxia), and areflexia. ...
    https://medlineplus.gov/genetics/condition/guillain-barre-syndrome - Genetics
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