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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Baishideng Publishing Group Inc
2023
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| Materias: | |
| 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 |