Familial mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode syndrome: Three case reports

BACKGROUND: Mitochondrial encephalomyopathy (ME) is a multisystem metabolic disease that primarily affects the central nervous system and skeletal muscle. It is caused by mutations in mitochondrial or nuclear DNA, resulting in abnormal mitochondrial structure and function and insufficient ATP synthe...

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Detalles Bibliográficos
Autores principales: Yang, Xiao, Fu, Le-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516927/
https://www.ncbi.nlm.nih.gov/pubmed/36186180
http://dx.doi.org/10.12998/wjcc.v10.i27.9945

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516927/
https://www.ncbi.nlm.nih.gov/pubmed/36186180
http://dx.doi.org/10.12998/wjcc.v10.i27.9945

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