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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Detalles Bibliográficos
Autores principales: Guerriero, Silvana, Vetrugno, Michele, Ciracì, Lorenza, Artuso, Lucia, Dell’Aglio, Rosa, Petruzzella, Vittoria
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085157/
https://www.ncbi.nlm.nih.gov/pubmed/21572739
http://dx.doi.org/10.4103/0974-9233.75892

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085157/
https://www.ncbi.nlm.nih.gov/pubmed/21572739
http://dx.doi.org/10.4103/0974-9233.75892

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