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DeCS
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Descriptor English:
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Ophthalmoplegia, Chronic Progressive External
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Descriptor Spanish:
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Oftalmoplejía Externa Progresiva Crónica
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Descriptor Portuguese:
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Oftalmoplegia Externa Progressiva Crônica
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Synonyms English:
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CPEO
Chronic Progressive External Ophthalmoplegia
Disease, Graefe
Dystrophy, Ocular Muscular
External Ophthalmoplegia, Progressive
Graefe Disease
Graefe's Disease
Mitochondrial Ocular Myopathy
Muscular Dystrophies, Ocular
Muscular Dystrophy, Ocular
Myopathy, Mitochondrial Ocular
Ocular Muscular Dystrophies
Ocular Muscular Dystrophy
Ocular Myopathy of Von Graefe Fuchs
Ocular Myopathy of Von Graefe-Fuchs
Ocular Myopathy, Mitochondrial
Ophthalmoplegia, Progressive External
Progressive External Ophthalmoplegia
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Tree Number:
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C05.651.460.700
C10.292.562.750.250
C10.597.622.447.511
C10.668.491.500.700
C11.590.472.250
C18.452.660.560.700
C23.888.592.636.447.511
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Definition English:
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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) |
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Indexing Annotation English:
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chronic progressive external ophthalmoplegia with cardiomyopathy & retinitis pigmentosa = KEARNS-SAYRE SYNDROME
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History Note English:
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93
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Allowable Qualifiers English:
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Record Number:
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30631
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Unique Identifier:
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D017246
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Occurrence in VHL:
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Similar:
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DeCS
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