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Updated: Jun 18, 2026

Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes
Published on: October 10, 2025
Heart diseases in mitochondrial encephalomyopathy, lactic acidosis, and stroke syndrome
1Critical Care Medicine, Boulevard Raymond-Poincare, Raymond Poincare Hospital, Garches, Ile de France 92380, France. fayssoil2000@yahoo.fr
Abstract:
Mitochondrial encephalomyopathy, lactic acidosis, and stroke (MELAS) syndrome is a mitochondrial genetic disorder caused by a point mutation, resulting in the substitution of guanine for adenine at nucleotide 3243 (A3243G) of mitochondrial DNA. This disease is characterized by a multisystem disorder with variable manifestations. The authors review heart involvement in this disease.
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