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Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes
Published on: October 10, 2025
Mitochondrial encephalomyopathies and related syndromes: brief review
Enrico Bertini1, Adele D'Amico
1Bambino Gesu' Children's Research Hospital, Department of Laboratory Medicine, Rome, Italy. ebertini@tin.it
Abstract:
A brief and comprehensive review on mitochondrial cytopathies is reported showing the extreme clinical and genetic heterogeneity of these disorders. Syndromes of mitochondrial cytopathiesencompass most of the medical specialties and diagnosis of mitochondrial cytopathies is complicated,needing the combination of multiple expertise: muscle morphology, neuroradiology, biochemistry(enzymology, chemical analysis), and genetics.
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