NI-19 A case of Leber’s hereditary optic neuropathy with diffuse white matter changes mimicking gliomatosis cerebri

BACKGROUND: Leber’s hereditary optic neuropathy (LHON) is a mitochondrial disease characterized by bilateral severe subacute central vision loss and a mutation in the mitochondrial DNA (mtDNA). The cranial magnetic resonance imaging (MRI) of LHON patients varies from subtle to multiple white matter...

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Detalles Bibliográficos
Autores principales: Saruta, Wakiko, Shibahara, Ichiyo, Inukai, Madoka, Kanayama, Shunsuke, Akiyama, Hisanao, Ishikawa, Hitoshi, Sato, Sumito, Hide, Takuichiro, Kumabe, Toshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Supplement Abstracts
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648173/
http://dx.doi.org/10.1093/noajnl/vdab159.080

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