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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Detalhes bibliográficos
Main Authors: Guerriero, Silvana, Vetrugno, Michele, Ciracì, Lorenza, Artuso, Lucia, Dell’Aglio, Rosa, Petruzzella, Vittoria
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications 2011
Assuntos:
Case Report
Acesso em linha: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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