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Concept information

Nervous System Diseases > Cranial Nerve Diseases > Ocular Motility Disorders > Ophthalmoplegia > Ophthalmoplegia, Chronic Progressive External
Eye Diseases > Ocular Motility Disorders > Ophthalmoplegia > Ophthalmoplegia, Chronic Progressive External
Nervous System Diseases > Neurologic Manifestations > Paralysis > Ophthalmoplegia > Ophthalmoplegia, Chronic Progressive External
Musculoskeletal Diseases > Muscular Diseases > Mitochondrial Myopathies > Ophthalmoplegia, Chronic Progressive External
Nervous System Diseases > Neuromuscular Diseases > Muscular Diseases > Mitochondrial Myopathies > Ophthalmoplegia, Chronic Progressive External

Preferred term

Ophthalmoplegia, Chronic Progressive External  

Type

  • mesh:Descriptor

Definition

  • A mitochondrial myopathy characterized by slowly progressive paralysis of the levator palpebrae, orbicularis oculi, and extraocular muscles. Ragged-red fibers and atrophy are found on muscle biopsy. Familial and sporadic forms may occur. Disease onset is usually in the first or second decade of life, and the illness slowly progresses until usually all ocular motility is lost. (From Adams et al., Principles of Neurology, 6th ed, p1422)

Narrower concepts

Entry terms

  • Chronic Progressive External Ophthalmoplegia
  • CPEO
  • Graefe Disease
  • Graefe's Disease
  • Mitochondrial Ocular Myopathy
  • Ocular Muscular Dystrophy
  • Ocular Myopathy of Von Graefe-Fuchs
  • Ophthalmoplegia, Progressive External
  • Progressive External Ophthalmoplegia

In other languages

  • French

  • Dystrophie musculaire oculaire
  • Myopathie oculaire mitochondriale
  • OEP (Ophtalmoplégie Externe Progressive)
  • Ophtalmoplégie externe progressive chronique
  • Syndrome de von Graefe

URI

http://data.loterre.fr/ark:/67375/JVR-ZRG0L5X5-R

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