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Catatonia and Mitochondrial Dysfunction in a Young Female with MT-ND3 Mutation: A Case Report and Literature Review

2025-08-19

Abstract excerpt

<h4>Introduction: </h4> Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes (MELAS) is a rare multisystem mitochondrial disorder primarily caused by mutations in mitochondrial DNA. While it typically presents with stroke-like episodes, seizures, and lactic acidosis, recent evidence highlights a broader clinical spectrum including neuropsychiatric manifestations. Case Presentation: We report...

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Literature Corpus work
a83f6db0-3dcb-53dc-af3b-ce26ecc547df
DOI
10.22541/au.175564274.49735147/v1
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Catatonia and Mitochondrial Dysfunction in a Young Female with MT-ND3 Mutation: A Case Report and Literature ReviewDOI 10.22541/au.175564274.49735147/v1
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