About: Leber's hereditary optic nerve neuropathy     Goto   Sponge   NotDistinct   Permalink

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Description
  • The authors present a case report of 26 years old man with bilateral optic nerve neuropathy. Detection of heteroplasmic mutation of mitochondrial DNA at G3460A site confirmed the suspicion on Lebers hereditary optic nerve neuropathy (LHON). Genetic and environmental factors of the disease and various accompanying neurologic and other symptoms, which can together with the optic nerve defect participate in the development of of the LOHN clinical pattern are discussed. (en)
  • Autoři předkládají studii 26-ti letého muže s oboustrannou atrofií optického nervu. U pacienta byla diagnostikována Leberova hereditální optická neuropatie s mtDNA mutací v pozici G3460A. Jsou zhodnoceny genetické factory a faktory prostředí, které se mohou spolupodílet na rozvoji klinického obrazu onemocnění.
Title
  • Leber's hereditary optic nerve neuropathy (en)
  • Leberova hereditarna neuropatia zrakoveho nervu.
skos:prefLabel
  • Leber's hereditary optic nerve neuropathy (en)
  • Leberova hereditarna neuropatia zrakoveho nervu.
skos:notation
  • RIV/67985823:_____/99:03!RIV/2002/MSM/A20002/N
http://linked.open.../vavai/riv/strany
  • 598-600
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  • P(ME 256)
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  • 11
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  • 744613
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  • RIV/67985823:_____/99:03
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  • Slepota, LHON, mtDNA, mutace G3460A, mutace G11778A, heteroplazmie. (en)
http://linked.open.../riv/klicoveSlovo
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  • SK - Slovenská republika
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  • [00CC403DFE7C]
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  • Bratislavské lékařské listy
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http://linked.open...v/svazekPeriodika
  • 100
http://linked.open...iv/tvurceVysledku
  • Houštěk, Josef
issn
  • 0006-9248
number of pages
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