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2024-05-31
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Articles
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CARDIOLOGY AND GENETICS
Rano Berdieva
Termez branch of the Tashkent Medical Academy
Zokir Norkulov
Termez branch of the Tashkent Medical Academy
Dilbar Nuralieva
Termez branch of the Tashkent Medical Academy
##semicolon## hypertrophic cardiomyopathy, dilated cardiomyopathy, channelopathies, arrhythmogenic cardiomyopathy, pulmonary hypertension, genetic myocardial diseases, Congress “Genetics and the Heart”
सार
Hereditary cardiovascular diseases make a significant contribution to the structure of cardiovascular pathology. The article is devoted to a review of materials on genetically determined cardiac diseases, which were discussed at the First International Congress “Genetics and the Heart”. The most current data on hypertrophic and dilated cardiomyopathies and hereditary problems of arrhythmogenesis are presented. The main participants of the congress are listed
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Charron P, Arad M, Monserrat L et al. Genetic counselling and testing in cardiomyopathies: A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J 2010; 31 (22): 2715–28.
Ackerman М et al. HRS/EHRA Expert Consensus Statement on Genetic Testing. Heart Rhythm 2011; 8 (8).
Elliott PM, Anastasakis A, Borger MA et al. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: The Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). Eur Heart J 2014; 35 (39): 2733–79.
Jan Haas et al. Atlas of the clinical genetics of human dilated cardiomyopathy. Eur Heart J 2015; 36: 1123–35.
Priori SG et al. 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death. Eur Heart J 2015; 8 (9): 746–837.
Manonelles P et al. Estudio de la muertesúbita en deportistas españoles. Investig Cardiovasc 2006; 9 (1): 55–73.
Hayashi M et al. The spectrum of epidemiology underlying sudden cardiac death. Circ Res 2015; 116: 1887–906.
Monserrat L. Perspectives on current recommendations for genetic testing in HCM. GCSP 2018; 23.
Cerrone M, Priori SG. Genetics of sudden death: focus on inherited channelopathies. Eur Heart J 2011; 32: 2109–18. DOI: 10.1093/eurheartj/ehr082
Bezzina CR, Lahrouchi N, Priori SG. Genetics of Sudden Cardiac Death. Circulation 2015; 116: 1919–36. DOI: 10.1161/CIRCRESAHA.116.304030
Charron P, Carrier L, Dubourg O et al. Penetrance of familial hypertrophic cardiomyopathy. Genet Couns 1997; 8: 107–14.
Maron BJ, Maron MS, Semsarian C. Double or compound sarcomere mutations in hypertrophic cardiomyopathy: a potential link to sudden death in the absence of conventional risk factors. Heart Rhythm 2012; 9: 57–63. DOI: 10.1016/j.hrthm.2011.08.009
