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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Autori principali: Guerriero, Silvana, Vetrugno, Michele, Ciracì, Lorenza, Artuso, Lucia, Dell’Aglio, Rosa, Petruzzella, Vittoria
Natura: Artigo
Lingua:Inglês
Pubblicazione: Medknow Publications 2011
Soggetti:
Case Report
Accesso online: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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