Isolated and repeated stroke-like episodes in a middle-aged man with a mitochondrial ND3 T10158C mutation: a case report

BACKGROUND: Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome, is the most common phenotype of mitochondrial disease. It often develops in childhood or adolescence, usually before the age of 40, in a maternally-inherited manner. Mutations in mitochondr...

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Detalhes bibliográficos
Publicado no:BMC Neurol
Main Authors: Mezuki, Satomi, Fukuda, Kenji, Matsushita, Tomonaga, Fukushima, Yoshihisa, Matsuo, Ryu, Goto, Yu-ichi, Yasukawa, Takehiro, Uchiumi, Takeshi, Kang, Dongchon, Kitazono, Takanari, Ago, Tetsuro
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5729248/
https://ncbi.nlm.nih.gov/pubmed/29237403
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-017-1001-4
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