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Case Study: Familial Hypertrophic Cardiomyopathy

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Familial hypertrophic cardiomyopathy

Familial hypertrophic cardiomyopathy is a heart condition which affects 1 in every 500 people, being the most common genetic heart disease. Symptoms of this condition include thickening of the heart (cardiac) muscles (see fig. 1). This usually occurs within the inter ventricular septum which is the muscle wall that separates the two lower chambers of the heart [ USA.gov, August 2015]. The condition becomes dangerous when the thickened muscle prevents or slows the flow of oxygenated blood to the body [National Heart, Lung and Blood Institute, 2016]

It is common for Hypertrophic cardiomyopathy to develop in adolescence or during young adulthood, although it can be developed at any age. The symptoms of this

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