Hypertrophic cardiomyopathy (HCM) is a genetic heart disorder affecting approximately 1 in 500 people worldwide. Despite its relatively high prevalence, HCM often goes undiagnosed due to subtle or absent early symptoms. The condition involves abnormal thickening of the heart muscle, particularly the ventricles, which can impede normal blood flow and increase the risk of sudden cardiac events. Early detection is critical, yet many individuals remain unaware of their risk until complications arise, underscoring the importance of recognizing early warning signs and improving diagnostic approaches.
Health
Conclusion Recognizing early symptoms of hypertrophic cardiomyopathy (HCM) is critical for timely intervention and prevention of serious complications. Because HCM can present subtly or fluctuate over…