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Adult-onset MELAS syndrome in a 51-year-old woman without typical clinical manifestations: a case report
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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
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 |