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Hypertrophic cardiomyopathy (HCM) is a common genetic cardiac disorder affecting 1 in 500 people. It affects both men and women of all ages, and is characterized by abnormal thickening of the heart muscle. The University of Michigan is one of only 14 clinics in the country specializing in the treatment of this challenging disorder, offering a multidisciplinary approach that is comprehensive in both diagnosis and treatment, and individualized for every patient.