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Results 1 - 10 of 11 for Progressive ophthalmoplegia
  1. Progressive external ophthalmoplegia 
    Progressive external ophthalmoplegia is a condition characterized by weakness of the eye muscles. The condition typically appears in adults ... slowly worsens over time. The first sign of progressive external ophthalmoplegia is typically drooping eyelids (ptosis), which can affect ...
    https://medlineplus.gov/.../progressive-external-ophthalmoplegia - Genetics
  2. Progressive supranuclear palsy 
    ... each cell is sufficient to cause the disorder. Progressive supranuclear ophthalmoplegia PSP Richardson's syndrome Steele-Richardson-Olszewski syndrome ...
    https://medlineplus.gov/.../condition/progressive-supranuclear-palsy - Genetics
  3. Horizontal gaze palsy with progressive scoliosis 
    ... associated with bilateral paralysis of conjugate gaze HGPPS Progressive external ophthalmoplegia and scoliosis Genetic Testing Registry: Gaze palsy, familial ...
    https://medlineplus.gov/...tal-gaze-palsy-with-progressive-scoliosis - Genetics
  4. Ataxia neuropathy spectrum 
    ... and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. Neuromuscul Disord. 2003 Feb;13(2):133-42. ...
    https://medlineplus.gov/.../condition/ataxia-neuropathy-spectrum - Genetics
  5. Kearns-Sayre syndrome 
    ... and symptoms. People with Kearns-Sayre syndrome have progressive external ophthalmoplegia, which is weakness or paralysis of the eye ...
    https://medlineplus.gov/genetics/condition/kearns-sayre-syndrome - Genetics
  6. TK2-related mitochondrial DNA depletion syndrome, myopathic form 
    ... that control eye movement, leading to droopy eyelids (progressive external ophthalmoplegia).Most often in TK2-MDS, the muscles are ...
    https://medlineplus.gov/...ial-dna-depletion-syndrome-myopathic-form - Genetics
  7. Spinocerebellar ataxia type 1 
    ... type 1 (SCA1) is a condition characterized by progressive problems with ... (ophthalmoplegia). Eye muscle weakness leads to rapid, involuntary eye ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  8. Spinocerebellar ataxia type 2 
    ... type 2 (SCA2) is a condition characterized by progressive problems with movement. ... (ophthalmoplegia). Eye muscle weakness leads to involuntary back-and- ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  9. 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
  10. 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
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