Abstract
The term cardiomyopathy encompasses a heterogeneous group of disorders characterized by an intrinsic pathology of the cardiac muscle. Cardiomyopathies differ from other cardiac diseases in that they are not the result of other pathologies, such as pericardial diseases, hypertension, congenital abnormalities, valvulopathies or ischemic heart diseases. Diverse types of cardiomyopathies can be distinguished according to their morphology or aetiology. The major morphological patterns are: hypertrophic, dilated, restrictive, arrhythmogenic and non-compacted. Based on the aetiology, cardiomyopathies can be primary/secondary or familial/non-familial.
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Aguilera, B., Suárez-Mier, M.P., Guzzo-Merello, G., García-Pavía, P. (2015). Cardiomyopathies. In: Lucena, J., García-Pavía, P., Suarez-Mier, M., Alonso-Pulpon, L. (eds) Clinico-Pathological Atlas of Cardiovascular Diseases. Springer, Cham. https://doi.org/10.1007/978-3-319-11146-9_8
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