CURRENT STATE OF THE ART OF DILATED CARDIOMYOPATHY

dc.contributor.authorVakhidova Ikbolkhon Kholmurod qizi
dc.date.accessioned2025-12-31T15:37:57Z
dc.date.issued2023-10-21
dc.description.abstractThis 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.
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dc.identifier.urihttps://scholarexpress.net/index.php/wbph/article/view/3282
dc.identifier.urihttps://asianeducationindex.com/handle/123456789/49490
dc.language.isoeng
dc.publisherScholar Express Journals
dc.relationhttps://scholarexpress.net/index.php/wbph/article/view/3282/2798
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.sourceWorld Bulletin of Public Health; Vol. 27 (2023): WBPH; 63-66
dc.source2749-3644
dc.subjectCardiomyopathy
dc.subjectcongestive cardiomyopathy
dc.subjectmorphofunctional types
dc.subjectpharmacotherapy
dc.titleCURRENT STATE OF THE ART OF DILATED CARDIOMYOPATHY
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Article

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