نتایج جستجو برای: arrhythmogenic right ventricular dysplasia

تعداد نتایج: 433082  

Journal: :International Journal of Advances in Medicine 2023

Arrhythmogenic cardiomyopathy (ACM) is a progressive genetic disease of the myocardium characterized by loss myocardial cells and replacement fibrofatty tissue in right and/or left ventricle (RV/LV), clinically manifested syncope, palpitations, heart failure, or sudden cardiac death (SCD). We presented case where patient suffered from palpitations for previous three to four years, which resolve...

Journal: :Pakistan Heart Journal 2022

Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia (ARVD) is regarded to be one of the highest common cause death especially in athletes due sudden cardiac arrest. Epidemiologically, 1 among 5000 populations has estimated prevalence ARVD. ARVD clinical indications or symptoms before age 12 are difficult diagnose and it also rare acquire after 60. 34-year-old male patient with no-known co...

Journal: :the journal of tehran university heart center 0
farveh vakilian atherosclerosis prevention research center, imam reza hospital, mashhad university of medical sciences, mashhad, iran. mahmood mohamadzadeh shabestari atherosclerosis prevention research center, imam reza hospital, mashhad university of medical sciences, mashhad, iran. ahmad amin rajaie cardiovascular, medical and research center, iran university of medical sciences, tehran, iran. soheila chamanian atherosclerosis prevention research center, imam reza hospital, mashhad university of medical sciences, mashhad, iran. toktam moghiman atherosclerosis prevention research center, imam reza hospital, mashhad university of medical sciences, mashhad, iran.

arrhythmogenic right ventricular dysplasia/cardiomyopathy (arvd/c) is a congenital cardiac disease with myocardial involvement, most probably right ventricular (rv) dysfunction, accounting for 20% of sudden cardiac deaths. characterized by the fibro-fatty infiltration of the rv free wall, arvd/c presents in adolescents with ventricular arrhythmias and heart failure symptoms and as biventricular...

2011
Martina Perazzolo Marra Loira Leoni Barbara Bauce Alessandro Zorzi Manuel De Lazzari Francesco Corbetti Luisa Cacciavillani Ilaria Rigato Federico Migliore Maria Silvano Cristina Basso Francesco Tona Gianfranco Buja Gaetano Thiene Sabino Iliceto Domenico Corrado

Imaging study of ventricular scar in arrhythmogenic right ventricular cardiomyopathy/ dysplasia: comparison of three-dimensional electroanatomic voltage mapping and contrastenhanced cardiac magnetic resonance Martina Perazzolo Marra, Loira Leoni, Barbara Bauce, Alessandro Zorzi, Manuel De Lazzari, Francesco Corbetti, Luisa Cacciavillani, Ilaria Rigato, Federico Migliore, Maria Silvano, Cristina...

Journal: :Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 2014
Davide Moreira Anne Delgado Bruno Marmelo Emanuel Correia Pedro Gama João Pipa Luís Nunes Oliveira Santos

Arrhythmogenic right ventricular cardiomyopathy, also known as arrhythmogenic right ventricular dysplasia, is a condition in which myocardium is replaced by fibrous or fibrofatty tissue, predominantly in the right ventricle. It is clinically characterized by potentially lethal ventricular arrhythmias, and is a leading cause of sudden cardiac death. Its prevalence is not known exactly but is est...

Journal: :Circulation 2005
Rajeev K Pathak Fermin C Garcia

Endocardial and epicardial electroanatomical mapping and ablation is a safe and effective therapy in the treatment of right ventricle arrhythmias occurring in the setting of arrhythmogenic right ventricular cardiomyopathy (ARVD). Careful mapping and ablation plans must be tailored for each patient based on comorbidities and ventricular tachycardia morphologies. This review focuses on the cathet...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید