Treatment of a patient with severe lactic acidosis and multiple organ failure due to mitochondrial myopathy: A case report

BACKGROUND: Mitochondrial myopathy is a rare genetic disease with maternal inheritance that may involve multiple organ systems. Due to the lack of typical characteristics, its clinical diagnosis is difficult, and it is often misdiagnosed or even missed. CASE SUMMARY: The patient was a young college...

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Detalles Bibliográficos
Autores principales: Chen, Ling, Shuai, Tian-Kui, Gao, Yu-Wei, Li, Min, Fang, Peng-Zhong, Christian, Waydhas, Liu, Li-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445063/
https://www.ncbi.nlm.nih.gov/pubmed/37621593
http://dx.doi.org/10.12998/wjcc.v11.i22.5398

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445063/
https://www.ncbi.nlm.nih.gov/pubmed/37621593
http://dx.doi.org/10.12998/wjcc.v11.i22.5398

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