نتایج جستجو برای: arvd
تعداد نتایج: 232 فیلتر نتایج به سال:
Magnetic Resonance Imaging presentation of Arrhythmogenic Right Ventricular Dysplasia: a case report
Reprint requests to: Dr. Wen-Sheng Tzeng Department of Diagnostic Radiology, Chi-Mei Medical Center, Liou-Ying Campus. No. 201, Taikang Village, Liou-Ying, Tainan 736, Taiwan, R.O.C. Arrhythmogenic right ventricular dysplasia (A RV D) i s a non i schem ic c ard iomyopathy involving primarily the right ventricle. Its characteristics include hypokinetic areas involving the free wall of the right ...
BACKGROUND Management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is complicated by the incomplete information on the natural history of the disease and by the lack of risk stratification for cardiovascular death. The aim of the study was the identification of risk factors related to long-term prognosis. METHODS AND RESULTS Data were collected from 130 ...
OBJECTIVES The goal of this study was to analyze the genetic disorder of a family with cardiomyopathy, skin disorder, and woolly hair. BACKGROUND Arrhythmogenic right ventricular dysplasia (ARVD) is a heart muscle disorder causing arrhythmia and sudden cardiac death. We report a patient with familial autosomal recessive ARVD, woolly hair, and a pemphigous-like skin disorder with a new mutatio...
BACKGROUND The endocardial substrate for ventricular arrhythmias in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is thought to be caused by a progressive degenerative process. Many clinical decisions and treatment plans are guided by this pathophysiologic assumption, but the extent of progression of macroscopic endocardial scar and right ventricular (RV) dila...
Atherosclerotic renovascular disease (ARVD) continues to pose a thorny challenge for clinicians. ARVD remains themost prevalent cause of renal artery stenosis in Western countries and regularly accompanies disease in other vascular beds, including coronary, cerebral, aortic, and peripheral vessels. Not surprisingly, ARVD is associated with high risk for clinical events, including resistant hype...
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is characterised by morphological and histological changes in the ventricles. Progressive myocyte loss fibrofatty tissue replacement, producing islands of scar, can lead to reentrant tachycardia sudden cardiac death. It usually presents as chest pain, palpitations, heart failure, or syncope. The majority cases are seen before ag...
BACKGROUND Ventricular tachycardia (VT) ablation in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) has a low success rate. A more extensive epicardial (Epi) arrhythmogenic substrate could explain the low efficacy. We report the results of combined endocardial (Endo) and Epi VT ablation and conducting channel (CC) elimination. METHODS AND RESULTS Eleven consec...
AIMS We sought to determine the influence of genotype on clinical course and arrhythmic outcome among arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C)-associated mutation carriers. METHODS AND RESULTS Pathogenic mutations in desmosomal and non-desmosomal genes were identified in 577 patients (241 families) from USA and Dutch ARVD/C cohorts. Patients with sudden cardiac death...
The ideopatic VTs originated from RVOT usually carry only a low risk for syncope or SCD in the presence of structurally normal heart and myocardium. In contrast ARVD is a disease of the heart muscle associated with life-threatening ventricular arrhythmias and sudden death. It is characterised by structural and functional abnormalities of the right ventricle caused by the replacement of the myoc...
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