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Original Article

Clinical Features of Genetically Proved Leber Hereditary Optic Neuropathy in China

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Pages 207-210 | Accepted 15 Aug 2007, Published online: 08 Jul 2009

REFERENCES

  • Newman N J. Walsh and Hoyt Clinical Neuro-ophthalmology, 6th eds, N R Miller, N J Newman, V Biousse, J B Kerrison. Lippincott Williams & Wilkins, Baltimore 2005; 465–502
  • Wallace D C, Singh G, Lott M T, et al. Mitochondrial DNA mutation associated with Leber hereditary optic neuropathy. Science 1988; 242: 1427–1430
  • Newman N J, Lott M T, Wallace D C. The clinical characteristics of pedigree of Leber's hereditary optic neuropathy with the 11778 mutation. Am J Ophthalmol 1991; 111: 750–762
  • Johns D R, Smith K H, Miller N R. Leber's hereditary optic neuropathy. Clinical manifestation of the 3460 mutation. Arch Ophthalmol 1992; 110: 1577–158
  • Johns D R, Heher K L, Miller N R, Smith K H. Leber's optic neuropathy. Clinical manifestation of 14484 mutation. Arch Ophthalmol 1993; 111: 495–498
  • Riordan-Eva P, Harding A E. Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations. J Med Genet 1995; 32: 81–87
  • Brown M D, Wallace D C. Spectrum of mitochondrial DNA mutations in Leber's hereditary optic neuropathy. Clin Neurosci 1994; 2: 138–145
  • Hiida Y, Mashima Y, Oguchi Y, et al. Mitochondrial DNA analysis of Leber's hereditary optic neuropathy. Jpn J Ophthalmol 1991; 35(1)102–106
  • Mashima Y, Yamada K, Wakakura M, et al. Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese family with Leber's hereditary optic neuropathy. Curr Eye Res 1998; 17(4)403–408
  • Ishikawa S, Ichibe Y, Yokoe J, et al. Leber's hereditary optic neuropathy among Japanese. Clin Neurosci 1995; 3: S85–S89
  • Kim J Y, Hwang J M, Chang B L, et al. Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans. J Neurol 2003; 250(3)278–281
  • Yen M Y, Wang A G, Chang W L, et al. Leber's hereditary optic neuropathy-the spectrum of mitochondrial DNA mutations in Chinese patients. Jpn J Ophthalmol 2002; 46(1)45–51
  • Zhang L, Huang Y, Li F, et al. The mitochondrial DNA mutation at position 11778 in Chinese families with Leber's hereditary optic neuropathy. Yan Ke Xue Bao 1994; 10(3)151–156
  • Zhou X, Wei Q, Yang L, et al. Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families. Biochem Biophys Res Commun 2006; 340(1)69–75
  • Qu J, Li R, Zhou X, et al. The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation. Invest Ophthalmol Vis Sci 2006; 47(2)475–483
  • Jia X, Li S, Xiao X, et al. Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy. J Hum Genet 2006; 51(10)851–856
  • Qian Y, Zhou X, Hu Y, et al. Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy. Biochem Biophys Res Commun 2005; 332(2)614–616
  • Harding A E, Sweeney M G, Miller D H, et al. Occurrence o f a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Brain 1992; 115: 979–989
  • Jansen P H, Van der Knaap M S, de Coo I F. Leber's hereditary optic neuropathy with 11778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findings. J Neurol Sci. 1996; 135: 176–180
  • Vanopdenbosch L, Dubois B, D'Hooghe M B, et al. Mitochondrial DNA mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis. J Neurol. 2000; 247: 535–543

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