Adult-onset MELAS syndrome in a 51-year-old woman without typical clinical manifestations: a case report

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BACKGROUND: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome is a multi-organ disorder resulting from mitochondrial DNA (mtDNA) mutations. We report a case of suspected MELAS syndrome that progressed to left ventricular dysfunction 24 years after an init...

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Detalles Bibliográficos
Autores principales: Lee, Sang-Hyup, Lee, Chan Joo, Won, Dongju, Kang, Seok-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887669/
https://www.ncbi.nlm.nih.gov/pubmed/36733687
http://dx.doi.org/10.1093/ehjcr/ytad028

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