Comprehensive Diagnostic Criteria for MELAS Syndrome; a Case Study Involving an Elderly Patient With MT-TWm.5541C>T Mutation

The mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a matrilineal hereditary multisystem disease caused by mutations in the mitochondrial DNA. Although the initial diagnostic criteria correlate with a range of clinical phenotypes, including clinical onset...

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Detalles Bibliográficos
Autores principales: Wu, Gang, Shen, Yuguang, Zhu, Feng, Tao, Weiwei, Zhou, Yuanlin, Ke, Shaofa, Jiang, Huihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Case Report/Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158598/
https://www.ncbi.nlm.nih.gov/pubmed/36125978
http://dx.doi.org/10.1097/NRL.0000000000000457

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158598/
https://www.ncbi.nlm.nih.gov/pubmed/36125978
http://dx.doi.org/10.1097/NRL.0000000000000457

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