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Compressive Optic Neuropathy with a Concurrent Mutation of Leber’s Hereditary Optic Neuropathy: A Case Report
Leber’s hereditary optic neuropathy (LHON) is a mitochondrial genetic disease that leads to acute or subacute, painless, bilateral loss of vision, caused by degeneration of retinal ganglion cells that most affects men in their second or third decade of life. We describe a woman with compressive opti...
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| 出版年: | Neuroophthalmology |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Taylor & Francis
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7722701/ https://ncbi.nlm.nih.gov/pubmed/33335345 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/01658107.2019.1703197 |
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