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Even though hypertrophic cardiomyopathy (HCM) may be present early in life and is most likely congenital, it is one of the most-uncommon cardiac malformations encountered in pediatric cardiology, largely because the presentation of symptoms is usually absent, incomplete, or delayed into adulthood.
At the time of diagnosis, most people with hypertrophic cardiomyopathy will have no symptoms and no evidence of an obstruction. Apart from follow-up monitoring, most won’t require treatment.
Hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy develops when the walls of your left ventricle become thicker than normal. ... Symptoms of cardiovascular disease can vary depending on the ...
Hypertrophic cardiomyopathy screening [10] [11] Cardiomegaly (sometimes megacardia or megalocardia ) is a medical condition in which the heart becomes enlarged. It is more commonly referred to simply as "having an enlarged heart ".
Cardiomyopathy is a group of primary diseases of the heart muscle. [1] Early on there may be few or no symptoms. [1] As the disease worsens, shortness of breath, feeling tired, and swelling of the legs may occur, due to the onset of heart failure. [1]
Athlete's heart is not the cause of sudden cardiac death during or shortly after a workout, which mainly occurs due to hypertrophic cardiomyopathy and arrhythmogenic cardiomyopathy (ARVC), two genetic disorders. Although a link between intensive exercise and exercise-induced arrhythmogenic right ventricular cardiomyopathy exists. [3] [6]
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