Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report

BACKGROUND: Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode syndrome is a rare mitochondrial genetic disorder that can present with a variety of clinical manifestations, including stroke, hearing loss, seizures, and lactic acidosis. The most common genetic mutation associat...

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Detalles Bibliográficos
Autores principales: Alenezi, Ahmad F., Almelahi, Mariam A., Fekih-Romdhana, Feten, Jahrami, Haitham A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549677/
https://www.ncbi.nlm.nih.gov/pubmed/36210452
http://dx.doi.org/10.1186/s13256-022-03613-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549677/
https://www.ncbi.nlm.nih.gov/pubmed/36210452
http://dx.doi.org/10.1186/s13256-022-03613-2

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