Subclinical Leber’s hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eye

BACKGROUND: Leber’s hereditary optic neuropathy (LHON) is a mitochondrial disease characterized by visual loss consequent to optic nerve atrophy. In some cases, LHON is associated with heterogeneous neurological extraocular manifestations and is referred to as “Leber plus disease”; rarely it is asso...

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Detalles Bibliográficos
Autores principales: Mauri, Eleonora, Dilena, Robertino, Boccazzi, Antonio, Ronchi, Dario, Piga, Daniela, Triulzi, Fabio, Gagliardi, Delia, Brusa, Roberta, Faravelli, Irene, Bresolin, Nereo, Magri, Francesca, Corti, Stefania, Comi, Giacomo P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307307/
https://www.ncbi.nlm.nih.gov/pubmed/30591017
http://dx.doi.org/10.1186/s12883-018-1227-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307307/
https://www.ncbi.nlm.nih.gov/pubmed/30591017
http://dx.doi.org/10.1186/s12883-018-1227-9

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