Abstract
Dilated cardiomyopathy (DCM) is an increase in the size of the left and/or right ventricular cavity, with systolic dysfunction resulting in a decrease in ejection fraction. Atrial enlargement and valvular dysfunction may also be found. It can be the result of ischemic, toxic, viral, or genetic causes.
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McCourt, J., Richardson, R.R. (2017). Dilated Cardiomyopathy. In: Atlas of Acquired Cardiovascular Disease Imaging in Children. Springer, Cham. https://doi.org/10.1007/978-3-319-44115-3_25
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DOI: https://doi.org/10.1007/978-3-319-44115-3_25
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