Keywords :
Cardiomyopathy, Hypertrophic/complications/diagnosis/therapy; Death, Sudden/etiology/prevention & control; Humans; Risk Assessment; Risk Factors
Abstract :
[en] Hypertrophic cardiomyopathy is of genetic origin, characterized by asymmetric left ventricular hypertrophy and variable clinical presentation. The physiopathology includes diastolic dysfunction and, in one third of the patients, dynamic left ventricular outflow tract obstruction. Patients are at increased risk of sudden death. Risk stratification in the individual patient is an essential component of management. This article describes the clinical presentation of a patient and his mother and summarizes essential features of the disease and the current recommendations for the prevention of sudden cardiac death.
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