Evolution of clinical and genetic concepts of cardiomyopathies DOI Creative Commons
Olga Kovalyova, V.V. Nіkonov, Светлана Владимировна Иванченко

et al.

EMERGENCY MEDICINE, Journal Year: 2025, Volume and Issue: 21(1), P. 2 - 13

Published: March 15, 2025

The definitions and classifications of cardiomyopathies are presented from a historical perspective based on an analysis databases platforms such as PubMed, Web Science, Scopus, Google Scholar, using appropriate keywords. It is noted that the implementation high-tech research methods accompanied by creation concepts cardiomyopathies, establishing etiological pathogenetic links being transformed into clinical signs, which require stratification, risk factor assessment, prognosis. diagnostic value structural functional heart anomalies for ranking classical phenotypes dilated, hypertrophic, restrictive arrhythmogenic right ventricular cardiomyopathy аnalyzed. A description provided new phenotype non-dilated left syndromes associated with hypertrabeculation (non-compaction) takotsubo syndrome. possibilities genetic in determining primary factors myocardial damage, groups for-ming analyzed. prerequisite application laboratory practical work at family individual level genealogical, sex-age, phenotypic, other characteristics patients their relatives. determined interpretation results comprehensive examination complete testing provides fundamental base tools stratification symptoms differentiation timely measures to eliminate arrhythmias, prevent sudden cardiac death patients, providing consultation prognostic preventive medical recommendations members.

Language: Английский

Evolution of clinical and genetic concepts of cardiomyopathies DOI Creative Commons
Olga Kovalyova, V.V. Nіkonov, Светлана Владимировна Иванченко

et al.

EMERGENCY MEDICINE, Journal Year: 2025, Volume and Issue: 21(1), P. 2 - 13

Published: March 15, 2025

The definitions and classifications of cardiomyopathies are presented from a historical perspective based on an analysis databases platforms such as PubMed, Web Science, Scopus, Google Scholar, using appropriate keywords. It is noted that the implementation high-tech research methods accompanied by creation concepts cardiomyopathies, establishing etiological pathogenetic links being transformed into clinical signs, which require stratification, risk factor assessment, prognosis. diagnostic value structural functional heart anomalies for ranking classical phenotypes dilated, hypertrophic, restrictive arrhythmogenic right ventricular cardiomyopathy аnalyzed. A description provided new phenotype non-dilated left syndromes associated with hypertrabeculation (non-compaction) takotsubo syndrome. possibilities genetic in determining primary factors myocardial damage, groups for-ming analyzed. prerequisite application laboratory practical work at family individual level genealogical, sex-age, phenotypic, other characteristics patients their relatives. determined interpretation results comprehensive examination complete testing provides fundamental base tools stratification symptoms differentiation timely measures to eliminate arrhythmias, prevent sudden cardiac death patients, providing consultation prognostic preventive medical recommendations members.

Language: Английский

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