We report a case of a child, with a rare form of the idiopathic hypertrophic cardiomyopathy, associated with mid-cavity obstruction and high intraventricular peak pressure. Cardiomyopathy, diagnosed antenataly, was followed postnataly and, despite of a lot echocardiographic findings - the growing, development and clinical signs are minimal.
Key words: Hypertrophic cardiomyopathy, intraventricular pressure, left ventricle outlet tract obstruction, sudden death, echocardiography.
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