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This study investigates the prevalence of hypertrophic cardiomyopathy (HCM) in relatives of index patients with normal genetic investigations, finding that 60% of index patients had normal results and only 5% of their relatives were diagnosed with HCM. The majority of affected relatives were identified through family screening, and none experienced serious complications or sudden cardiac death during follow-up. The findings suggest that family screening in this context may have limited utility due to the lo

Author

mpmain1234

Language

EN