Leber’s hereditary optic neuropathy is multiorgan not mono-organ

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Leber’s hereditary optic neuropathy is multiorgan not mono-organ

Leber's hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disorder with bilateral loss of central vision primarily due to mitochondrial DNA (mtDNA) mutations in subunits of complex I in the respiratory chain (primary LHON mutations), while other mtDNA mutations can also be causative. Since the first description, it is known that LHON is not restricted to the eyes but is...

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[Leber's hereditary optic neuropathy].

233 personal cases of leber's optic neuropathy have been analyzed by the authors in order to present clinical symptoms, evolution and genetic aspects. A group of 23 patients, in which 7 presented the disease and the others were asymptomatic members of families with the disease, was analyzed on evaluation of abnormalities of evoked visual responses; An other similar group, in repartition of subj...

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Leber’s Hereditary Optic Neuropathy

Four new missense mutations have been identified through restriction analysis and sequencing of the mitochondrial DNAs (mtDNA) from Leber’s hereditary optic neuropathy (LHON) patients who lacked the previously identified 1 1778 mutation. Each altered a conserved amino acid and correiated with the LHON phenotype in population and phylogenetic analyses. The nucleotide pair (np) 13708 mutation (G ...

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Leber hereditary optic neuropathy

Leber hereditary optic neuropathy is a maternally inherited bilateral optic neuropathy that typically affects teenage males with acute vision loss first in one eye and then the other within days or weeks. The etiology involves a point mutation in the mitochondrial DNA at 1 of 3 main loci: 11778, 14484, or 3460. There are some distinctive changes in the ocular fundus appearance at various stages...

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ژورنال

عنوان ژورنال: Clinical Ophthalmology

سال: 2016

ISSN: 1177-5483

DOI: 10.2147/opth.s120197