Highlights a rare case of fetal-diagnosed hypertrophic cardiomyopathy with mid-cavity obstruction that remained clinically benign postnatally despite significant echocardiographic findings.
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.
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Bejiqi et al. (2011) studied this question.
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