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MELAS Syndrome Presenting with Hypertrophic Cardiomyopathy and Advanced Heart Failure: A Multisystem Diagnostic
Jozef Dodulík1,2, Marie Lazárová1,2, Eva Kapsová1,2
1Department of Internal Medicine and Cardiology, University Hospital Ostrava, 708 00 Ostrava, Czech Republic.
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) can present as cardiomyopathy. Early genetic testing is crucial for diagnosing this rare condition, especially with coexisting kidney and hearing issues.
Area of Science:
- Genetics
- Cardiology
- Neurology
Background:
- Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) is a rare genetic disorder.
- Cardiac involvement, including hypertrophic cardiomyopathy and heart failure, is often underrecognized in MELAS.
- The m.3243A>G variant in MT-TL1 is the most common cause of MELAS.
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