نتایج جستجو برای: arrhythmogenic right ventricular dysplasia

تعداد نتایج: 433082  

Journal: :Soudni lekarstvi 2013
Okan Akan Selçuk Cetin Bülent Eren Dilek Durak Nursel Türkmen Umit Naci Gündoğmuş

UNLABELLED Arrhythmogenic right ventricular dysplasia (ARVD) is both a myocardial disease that predominantly affects the right ventricle (RV) and one of the major causes of sudden death in the young and athletes. A 28-year-old man with no signicant medical history, applied to an emergency department with feeling very ill. After his initial examinations, electrocardiography (ECG) showed ventricu...

Journal: :Journal of the American College of Cardiology 2001
M Boulos I Lashevsky S Reisner L Gepstein

OBJECTIVES We tested the hypothesis that spatial association of low-amplitude intracardiac electrograms can identify the presence, location and extent of dysplastic regions in arrhythmogenic right ventricular dysplasia (ARVD). BACKGROUND Arrhythmogenic right ventricular dysplasia is a right ventricular (RV) cardiomyopathy characterized pathologically by fibrofatty infiltration and clinically ...

2009
Mark D. McCauley Xander H. T. Wehrens

Inherited arrhythmogenic cardiomyopathies are the most common cause of sudden cardiac death (SCD) in patients under 40 years of age. According to a recent expert consensus panel, cardiomyopathies are defined as ‘a heterogeneous group of diseases of the myocardium associated with mechanical and/or electrical dysfunction that usually exhibit inappropriate ventricular hypertrophy or dilatation, an...

Journal: :Revista espanola de cardiologia 2002
Daniel More Kevin O'Brien Janet Shaw

Arrhythmogenic right ventricular dysplasia (ARVD) is a syndrome characterized by recurrent ventricular tachycardia. However, cases of ARVD have also presented as dilated cardiomyopathy later associated with ventricular arrhythmias. Histologically, this syndrome manifests as a fibrofatty replacement of the RV myocardium, predisposing the heart to ventricular arrhythmias. ARVD was once considered...

Journal: :Journal of cardiovascular electrophysiology 2004
Chandra Bomma Julie Rutberg Harikrishna Tandri Khurram Nasir Ariel Roguin Crystal Tichnell Rene Rodriguez Cynthia James Edward Kasper Philip Spevak David A Bluemke Hugh Calkins

INTRODUCTION Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) has major implications for the management of patients and their first-degree relatives. Diagnosis is based on a set of criteria proposed by the International Task Force for Cardiomyopathies. We report our experience in providing a re-evaluation for patients who previously have been diagnosed with ARVD/C...

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