MELAS/LS Overlap Syndrome Associated With Mitochondrial DNA Mutations: Clinical, Genetic, and Radiological Studies

Introduction: Mitochondrial diseases are characterized by considerable clinical and genetic heterogeneity. Mitochondrial encephalomyopathy with lactate acidosis and stroke-like episodes (MELAS) and Leigh syndrome (LS) are both established mitochondrial syndromes; sometimes they can overlap. Methods:...

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Detalles Bibliográficos
Autores principales: Wei, Yanping, Huang, Yan, Yang, Yingmai, Qian, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8137909/
https://www.ncbi.nlm.nih.gov/pubmed/34025555
http://dx.doi.org/10.3389/fneur.2021.648740

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8137909/
https://www.ncbi.nlm.nih.gov/pubmed/34025555
http://dx.doi.org/10.3389/fneur.2021.648740

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