نتایج جستجو برای: arrhythmogenic right ventricular dysplasia
تعداد نتایج: 433082 فیلتر نتایج به سال:
[Prevailing right ventricular myocardiopathy for previous myocarditis or arrhythmogenic dysplasia?].
A clinical case of a 10-year-old male patient is reported. His dilated and prevailing right ventricular myocardiopathy shows diagnostic difficulties between previous myocarditis etiology and arrhythmogenic dysplasia. As the elements are not pathognomonic of one or other cause, the increase of cardiac enzymes in subacute stage maybe tends to the supposition of previous myocarditis. Hence, the qu...
Isolated manifestation of sarcoidosis in the heart is very rare. The present work describes the case of a 41-year-old woman with ventricular tachycardia and severe symptoms of heart failure in June 2006. Clinical, MRI and echocardiographic findings revealed the diagnosis of an arrhythmogenic right ventricular dysplasia. Due to the severe progression of the disease, cardiac transplantation was p...
A rrhythmogenic right ventricular cardiomyopathy/dyspla-sia (ARVC/D) is an inheritable heart muscle disease that predominantly affects the right ventricle (RV) and predisposes to ventricular arrhythmias and sudden cardiac death (SCD). In the last three decades, there have been a significant number of studies defining the pathogenesis, genetic aspects, and clinical manifestations of the disease ...
BACKGROUND The purpose of this study was to reevaluate the ECG features of arrhythmogenic right ventricular dysplasia (ARVD). The second objective was to evaluate the sensitivity and specificity of the standard and newly proposed diagnostic ECG markers in the presence of a right bundle-branch block (RBBB). METHODS AND RESULTS One hundred patients with ARVD (57 men; aged 39+/-15 years) and 57 ...
Arrhythmogenic right ventricular dysplasia (ARVD) is a recently described entity characterized by right ventricular myopathic changes and right ventricular tachycardia. The presence or extent of left ventricular dysfunction in ARVD is not known. We assessed right ventricular and left ventricular function and size in six patients with ARVD by echocardiography and radionuclide angiocardiography d...
Arrhythmogenic right ventricular dysplasia-cardiomyopathy (ARVD-C) is a rare heart condition with characteristic thinning and fibroadipose tissue replacement of the myocardium of the right ventricular wall. We have seen 20 autopsy cases with morphologic features fitting the criteria of ARVD-C in our hospital in the past 5 years. The clinical characteristics of these patients were not those desc...
1. Saguner AM, Duru F, Brunckhorst CB. Arrhythmogenic right ventricular cardiomyopathy: A challenging disease of the intercalated disc. Circulation 2013; 128: 1381 – 1386. 2. Saguner AM, Ganahl S, Kraus A, Baldinger SH, Medeiros-Domingo A, Saguner AR, et al. Clinical role of atrial arrhythmias in patients with arrhythmogenic right ventricular dysplasia. Circ J 2014; 78: 2854 – 2861. 3. Hulot JS...
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