Late-onset Mitochondrial Encephalomyopathy with Lactic Acidosis and Stroke-like Episodes (MELAS) Syndrome in a 63-year-old Patient

Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) usually manifests in early life. Clinical hallmarks of the disease are mitochondrial myopathies, encephalopathy with stroke-like episodes, seizures, and lactic acidosis. It rarely manifests in late adulthood. Here...

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Detalles Bibliográficos
Autores principales: Abdullah, Hassan, Shah, Syed, Husain, Humza, Hassan, Furqan, Maqsood, Hamza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255082/
https://www.ncbi.nlm.nih.gov/pubmed/32483512
http://dx.doi.org/10.7759/cureus.7862

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7255082/
https://www.ncbi.nlm.nih.gov/pubmed/32483512
http://dx.doi.org/10.7759/cureus.7862

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