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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 403-410 |
| Number of pages | 8 |
| Journal | Survey of Ophthalmology |
| Volume | 53 |
| Issue number | 4 |
| DOIs |
|
| State | Published - 2008 |
Keywords
- central scotoma
- Leber hereditary optic neuropathy
ASJC Scopus subject areas
- Ophthalmology
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