Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA

BACKGROUND: Leber's hereditary optic neuropathy (LHON) is a mitochondrial disorder with optic nerve atrophy. Although there are no other associated neurological abnormalities in most cases of LHON, cases of "LHON plus" have been reported. CASE REPORT: The proband was a 37-year-old man...

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Detalles Bibliográficos
Autores principales: Nakaso, Kazuhiro, Adachi, Yoshiki, Fusayasu, Emi, Doi, Koji, Imamura, Keiko, Yasui, Kenichi, Nakashima, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469805/
https://www.ncbi.nlm.nih.gov/pubmed/23091534
http://dx.doi.org/10.3988/jcn.2012.8.3.230

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