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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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Detalles Bibliográficos
Autores principales:	Mezuki, Satomi, Fukuda, Kenji, Matsushita, Tomonaga, Fukushima, Yoshihisa, Matsuo, Ryu, Goto, Yu-ichi, Yasukawa, Takehiro, Uchiumi, Takeshi, Kang, Dongchon, Kitazono, Takanari, Ago, Tetsuro
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729248/ https://www.ncbi.nlm.nih.gov/pubmed/29237403 http://dx.doi.org/10.1186/s12883-017-1001-4

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