Table 1. Cardiac conditions that increase young athletes’ risk for SCD.
Anomalous origin of coronary artery (second most common cause in the United States) |
Aortic valve stenosis |
Aortic dissection (usually complication in Marfan syndrome) |
Arrhythmogenic right ventricular cardiomyopathy (ARVC) (most common cause in Italy) |
Brugada syndrome (more prevalent in those of Asian descent) |
HCM |
Dilated cardiomyopathy |
Coarctation of aorta |
Congenital heart block (Mobitz type II, complete, or third degree) |
Congenital or acquired long QT syndromes |
Short QT syndrome |
Coronary artery disease (rare in those younger than 35) |
Restrictive cardiomyopathy |
Endocarditis |
Ehlers-Danlos syndrome |
Mitral valve prolapse |
Myocarditis |
Pericarditis |
Postoperative congenital heart disease |
Status post heart transplant |
Kawasaki disease (coronary artery abnormalities) |
Wolff-Parkinson-White syndrome |
SCD, sudden cardiac death; HCM, hypertrophic cardiomyopathy.