CURRENT STATE OF THE ART OF DILATED CARDIOMYOPATHY

loading.default
thumbnail.default.alt

item.page.date

item.page.journal-title

item.page.journal-issn

item.page.volume-title

item.page.publisher

Scholar Express Journals

item.page.abstract

This article based on disease “Cardiomyopathy which is an acute, subacute or chronic lesion of the heart muscle of unknown or unclear etiology, often combined with damage to the endocardium, and sometimes the pericardium.” His basic research has made significant contributions to the study of cardiomyopathy. In subsequent years, heated discussions arose about the nature of this disease and its classification, which served as the reason for the creation in 1980 of a committee for the study of ILC. Depending on the leading pathophysiological mechanism or, if possible, etiological (pathogenetic) factor, they are divided into four forms: dilated, hypertrophic, restrictive CMP and arrhythmogenic right ventricular CMP. Along with four nonspecific cardiomyopathies, including dilated, hypertrophic, restrictive, right ventricular arrhythmogenic dysplasia, as before, specific cardiomyopathies were identified and unclassified cardiomyopathies.

item.page.description

item.page.citation

item.page.collections

item.page.endorsement

item.page.review

item.page.supplemented

item.page.referenced