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Article

Clinical and Genetic Heterogeneity of HCM: The Possible Role of a Deletion Involving MYH6 and MYH7

10 Feb 2025

Abstract excerpt

BACKGROUND/OBJECTIVES: Pediatric hypertrophic cardiomyopathy (HCM) is the most common genetic myocardial disorder in children and a leading cause of sudden cardiac death (SCD) among the young. Its phenotypic variability, driven by incomplete penetrance and variable expressivity, presents significant challenges in diagnosis and clinical management. METHODS: In this study, we report a unique case of a 16-month-old...

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Share to Cardiac electrophysiology and arrhythmias
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PMID: 40004541
DOI: 10.3390/genes16020212

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