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A 15-year-old male came to our clinic because his father had died suddenly with a previous diagnosis of apical hypertrophic cardiomyopathy at age 38. His father’s records said he had congestive heart failure, a maximal left ventricular wall thickness of 28 mm, biventricular systolic dysfunction and left atrial hypertrophy on echocardiography. A female cousin of the …
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