Leber’s hereditary optic neuropathy with diffuse white matter changes mimicking gliomatosis cerebri: illustrative case

BACKGROUIND: 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 findings on cranial magnetic resonance imaging of patients with LHON vary from subtle to multiple whi...

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Detalles Bibliográficos
Autores principales: Saruta, Wakiko, Shibahara, Ichiyo, Handa, Hajime, Inukai, Madoka, Kanayama, Shunsuke, Yasumoto, Ryoma, Sakurai, Keizo, Akiyama, Hisanao, Ishikawa, Hitoshi, Sato, Sumito, Hide, Takuichiro, Kumabe, Toshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association of Neurological Surgeons 2021
Materias:
Case Lesson
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245756/
https://www.ncbi.nlm.nih.gov/pubmed/35854899
http://dx.doi.org/10.3171/CASE21161

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