Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome: A case-report and literature review (CARE-complaint)

RATIONALE: Mitochondrial encephalomyopathy with lactic acidosis and stroke- like episodes (MELAS) syndrome is caused by mitochondrial respiratory chain dysfunction and oxidative phosphorylation disorder. It is a rare clinical metabolic disease involved with multiple systems. PATIENT CONCERNS: A 22-y...

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Detalles Bibliográficos
Autores principales: Wang, Shuai, Song, Tao, Wang, Suping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302614/
https://www.ncbi.nlm.nih.gov/pubmed/32541454
http://dx.doi.org/10.1097/MD.0000000000020310

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302614/
https://www.ncbi.nlm.nih.gov/pubmed/32541454
http://dx.doi.org/10.1097/MD.0000000000020310

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