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Bilateral Progressive Visual Loss in an Epileptic, Mentally Retarded Boy
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited, monosymptomatic disorder, characterized by severe central vision loss and optic atrophy that most frequently affects young men. The classic LHON phenotype is associated to three mitochondrial DNA mutations, mostly homoplasmic, in...
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| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3085157/ https://ncbi.nlm.nih.gov/pubmed/21572739 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0974-9233.75892 |
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