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Macular thickness changes in a patient with Leber’s hereditary optic neuropathy
BACKGROUND: Leber’s hereditary optic neuropathy (LHON) refers to an optic nerve dysfunction due to mutations in the mitochondrial DNA, resulting in visual loss by apoptosis of retinal ganglion cells (RGC). In 20% of LHON cases, their fundus examination looks entirely normal at early stage. There are...
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| Publicado no: | BMC Ophthalmol |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4373513/ https://ncbi.nlm.nih.gov/pubmed/25885098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12886-015-0015-1 |
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