| KSS | Kearns-Sayre syndrome; Kearns-Sayre-Shy [syndrome] |
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| K-S | Kearns-Sayre [syndrome] |
| Kearns | Thomas P., U.S. Ophthalmologist, *1922. See: Kearns-Sayre syndrome. (05 Mar 2000) |
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| kearns syndrome | <syndrome> A triad of progressive external ophthalmoplegia, cardiomyopathy, and retinitis pigmentosa. (12 Dec 1998) |
| Kearns-Sayre syndrome | <syndrome> A form of chronic progressive external ophthalmoplegia with associated cardiac conduction defects, short stature, and hearing loss; a sporadically ocurring mitochondrial myopathy presenting in childhood. (05 Mar 2000) |
Synonyms : Kearn-Sayre Mitochondrial Cytopathy, Kearns' Syndrome, Kearns-Sayre-Shy-Daroff Syndrome, Cytopathy, Kearn-Sayre Mitochondrial, Kearn Sayre Mitochondrial Cytopathy, Kearn Syndrome, Kearns Sayer Syndrome, Kearns Sayre Shy Daroff Syndrome, Syndrome, Kearns
| Kearns-Sayre syndrome |
Rare neuromuscular disorder characterized by heart disease, progressive paralysis of certain eye muscles, abnormal accumulation of colored material on the membrane lining of the eyes which leads to inflammation, degeneration, and wearing away of certain eye structures.
Ãâó: www.sparkle.usu.edu/glossary/syndromes_glossary.as...
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| Kearns-Sayre s. |
progressive ophthalmoplegia, pigmentary degeneration of the retina, myopathy, ataxia, and cardiac conduction defect; onset is before age 20. Almost all patients have large mitochondrial DNA deletions, and ragged red fibers are seen on muscle biopsy. Called also ophthalmoplegia plus.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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