Young onset mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome: a case report.

Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome (MELAS) is a rare mitochondrial disorder characterised by diverse neurological and systemic manifestations. The key underlying mechanism of the disease is related to protein synthesis, energy depletion, and nitric ox...

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Main Authors: Kartik Goel, Divyanshu Singh, Ravi Bhargav, Harsh Kansagara, Shailesh Kumar, Rupesh Yadav
Format: Article
Language:English
Published: Towarzystwo Pomocy Doraźnej 2024-12-01
Series:Critical Care Innovations
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Online Access:https://www.irdim.net/cci/7(4)43-48.html
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