Dear Editor,We read with interest the article by Liu et al[1]about an optical coherence tomography(OCT)study of five patients(10 eyes)with Leber’s hereditary optic neuropathy(LHON)due to the variant m.11778 G>A in...Dear Editor,We read with interest the article by Liu et al[1]about an optical coherence tomography(OCT)study of five patients(10 eyes)with Leber’s hereditary optic neuropathy(LHON)due to the variant m.11778 G>A in MT-ND4 which were compared with 11 clinically unaffected carriers(22 eyes)of the variant and with 20 healthy controls.展开更多
Leber’s hereditary optic neuropathy (LHON) causes central vision loss from bilateral optic neuropathy. Although 13 mitochondrial DNA (mtDNA)mutations are strongly associated with LHON, only three account for roughly ...Leber’s hereditary optic neuropathy (LHON) causes central vision loss from bilateral optic neuropathy. Although 13 mitochondrial DNA (mtDNA)mutations are strongly associated with LHON, only three account for roughly 90%of cases and thus are found inmultiple independent LHON families. The remaining LHON mutations are rare. Here, we describe the clinical and genetic characterization of a new LHON mtDNA mutation. The 12848T mutation alters a highly conserved amino acid in the ND5 complex I gene, is not found in controls, and is heteroplasmic. Despite ND5 being the largest of the mtDNA complex I genes, ND5 mutations are quite rare in LHON.展开更多
文摘Dear Editor,We read with interest the article by Liu et al[1]about an optical coherence tomography(OCT)study of five patients(10 eyes)with Leber’s hereditary optic neuropathy(LHON)due to the variant m.11778 G>A in MT-ND4 which were compared with 11 clinically unaffected carriers(22 eyes)of the variant and with 20 healthy controls.
文摘Leber’s hereditary optic neuropathy (LHON) causes central vision loss from bilateral optic neuropathy. Although 13 mitochondrial DNA (mtDNA)mutations are strongly associated with LHON, only three account for roughly 90%of cases and thus are found inmultiple independent LHON families. The remaining LHON mutations are rare. Here, we describe the clinical and genetic characterization of a new LHON mtDNA mutation. The 12848T mutation alters a highly conserved amino acid in the ND5 complex I gene, is not found in controls, and is heteroplasmic. Despite ND5 being the largest of the mtDNA complex I genes, ND5 mutations are quite rare in LHON.
