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AIM: To assess the effect of heteroplasmy on the expression of Leber's hereditary optic neuropathy (LHON) in a large family with the 3460 LHON mutation. METHODS: Mutation detection was performed by restriction enzyme digestion of polymerase chain reaction (PCR) products. Heteroplasmy was estimated by quantitation of wild type:mutant product ratios. RESULTS: There is a significant association between levels of mutant mtDNA and manifestation of the disease phenotype. CONCLUSION: As a high proportion of families with the 3460 mutation demonstrate heteroplasmy; this is likely to be a significant factor in disease expression.

Original publication

DOI

10.1136/bjo.80.10.915

Type

Journal article

Journal

Br J Ophthalmol

Publication Date

10/1996

Volume

80

Pages

915 - 917

Keywords

Adolescent, Adult, Aged, Aged, 80 and over, DNA Mutational Analysis, DNA, Mitochondrial, Female, Humans, Male, Middle Aged, Mutation, Optic Atrophies, Hereditary, Pedigree, Phenotype, Polymerase Chain Reaction