Cardiac Involvement in Patients with MELAS-Related mtDNA 3243A>G Variant

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare disease with variable clinical manifestations. MELAS is most often caused by the human mitochondrial DNA (mtDNA) m.3243A>G variant. We describe cardiac magnetic resonance (CMR) imaging fin...

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Bibliographic Details
Main Authors: Aino-Maija Vuorinen, Lauri Lehmonen, Mari Auranen, Sini Weckström, Sari Kivistö, Miia Holmström, Tiina Heliö
Format: Article
Language:English
Published: MDPI AG 2025-06-01
Series:Cardiogenetics
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Online Access:https://www.mdpi.com/2035-8148/15/2/16
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