| Literature DB >> 18572056 |
Vinay A Shah1, Sandeep Randhawa, Thomas Mizen, Andrew G Lee, Rod Foroozan.
Abstract
Leber hereditary optic neuropathy (LHON) produces a subacute and typically bilateral but sequential optic neuropathy. LHON is a mitochondrial disease and the most common mutations are at positions 11778, 14484 and 3460. LHON typically presents in young (age 20-40), healthy men but may occur in either sex and at any age. We report a case of LHON in a 72-year-old man and we emphasize the importance of testing for LHON in all cases of unexplained bilateral and sequential optic neuropathy with a ceco-central or central scotoma.Entities:
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Year: 2008 PMID: 18572056 DOI: 10.1016/j.survophthal.2008.04.003
Source DB: PubMed Journal: Surv Ophthalmol ISSN: 0039-6257 Impact factor: 6.048