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Dilated Cardiomyopathy With Hypergonadotropic Hypogonadism

Dilated Cardiomyopathy With Hypergonadotropic Hypogonadism

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Dilated Cardiomyopathy With Hypergonadotropic Hypogonadism: Understanding the Condition 1. Introduction Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism (DCM-HH) is a rare genetic disorder characterized by the development of dilated cardiomyopathy, a condition where the heart becomes enlarged and weakened, and hypergonadotropic hypogonadism, a condition where the sex glands produce little or no hormones. 2. Symptoms The symptoms…