Highlights & Basics
- Hypertrophic cardiomyopathy (HCM) is the most common cardiomyopathy and the most frequent cause of sudden cardiac death in young people.
- Presentation varies from asymptomatic to symptoms of heart failure.
- Physical examination may be normal at rest. Auscultation along the left sternal border when the patient is standing after a brief period of exercise may elicit a murmur.
- Family history may be present. Echocardiography should be used to screen first-degree family members.
- Has a benign prognosis in the majority of patients.
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O'Mahony C, Jichi F, Pavlou M, et al. A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD). Eur Heart J. 2014 Aug 7;35(30):2010-20.[Abstract][Full Text]
Pelliccia A, Sharma S, Gati S, et al. 2020 ESC guidelines on sports cardiology and exercise in patients with cardiovascular disease. Eur Heart J. 2021 Jan 1;42(1):17-96.[Abstract][Full Text]
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