نتایج جستجو برای: arvd

تعداد نتایج: 232  

Journal: :Circulation. Cardiovascular imaging 2010
Aditya Jain Monda L Shehata Matthias Stuber Seth J Berkowitz Hugh Calkins João A C Lima David A Bluemke Harikrishna Tandri

BACKGROUND Although arrhythmogenic right ventricular dysplasia (ARVD) predominantly affects the right ventricle (RV), genetic/molecular and histological changes are biventricular. Regional left ventricular (LV) function has not been systematically studied in ARVD. METHODS AND RESULTS The study population included 21 patients with suspected ARVD who underwent evaluation with MRI including tagg...

Journal: :Journal of the American College of Cardiology 2005
Harikrishna Tandri Manoj Saranathan E Rene Rodriguez Claudia Martinez Chandra Bomma Khurram Nasir Boas Rosen João A C Lima Hugh Calkins David A Bluemke

OBJECTIVES We evaluated the role of myocardial delayed-enhancement (MDE) magnetic resonance imaging (MRI) for noninvasive detection of fibrosis in Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). BACKGROUND Arrhythmogenic right ventricular dysplasia/cardiomyopathy is characterized by fibro-fatty replacement of the right ventricle (RV) leading to arrhythmias and RV failure. ...

Journal: :European journal of echocardiography : the journal of the Working Group on Echocardiography of the European Society of Cardiology 2004
Siddiq I Khalil Amjad Kamal Shakeel Ahmad

Arrhythmogenic right ventricular dysplasia (ARVD) is underdiagnosed cardiomyopathy which commonly presents in young adults with ventricular tachycardia or sudden death. We report a case of ARVD presenting with features of acute coronary syndrome. The suspicion of ARVD came only when echocardiogram revealed abnormal shape and wall motion of right ventricle, which was later confirmed by right ven...

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...

2016
Josef Finsterer Claudia Stöllberger

OBJECTIVES Arrhythmogenic right ventricular dysplasia (ARVD) is a rare, genetic disorder predominantly affecting the right ventricle. There is increasing evidence that in some cases, ARVD is due to mutations in genes, which have also been implicated in primary myopathies. This review gives an overview about myopathy-associated ARVD and how these patients can be managed. METHODS A literature r...

2001
F Niroomand N Trevisi P Della Bella

Background: Idiopathic right ventricular arrhythmias (IRVA) are responsive to medical and ablative treatment and have a benign prognosis. Arrhythmias caused by right ventricular dysplasia (ARVD) are refractory to treatment and may cause sudden death. It is difficult to distinguish between these two types of arrhythmia. Objective: To differentiate patients with IRVA and ARVD by a conventional el...

2010
Aimé Bonny Nicolas Lellouche Ivo Ditah Françoise Hidden-Lucet Martial T. Yitemben Benjamin Granger Fabrice Larrazet Robert Frank Guy Fontaine

Background. The relationship between C-reactive protein (CRP) elevation and ventricular tachycardia (VT) in arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is unclear. Methods and Results. In 91 consecutive patients with either ARVD/C with or without VT (cases) or idiopathic right ventricular outflow tract (RVOT) tachycardia (controls), blood sampling were taken to determine ...

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: :Circulation. Cardiovascular genetics 2009
Zahurul A Bhuiyan Jan D H Jongbloed Jasper van der Smagt Paola M Lombardi Ans C P Wiesfeld Marcel Nelen Meyke Schouten Roselie Jongbloed Moniek G P J Cox Marleen van Wolferen Luz M Rodriguez Isabelle C van Gelder Hennie Bikker Albert J H Suurmeijer Maarten P van den Berg Marcel M A M Mannens Richard N W Hauer Arthur A M Wilde J Peter van Tintelen

BACKGROUND This study aimed to evaluate the prevalence and type of mutations in the major desmosomal genes, Plakophilin-2 (PKP2), Desmoglein-2 (DSG2), and Desmocollin-2 (DSC2), in arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) patients. We also aimed to distinguish relevant clinical and ECG parameters. METHODS AND RESULTS Clinical evaluation was performed according to the ...

Journal: :Pacing and clinical electrophysiology : PACE 1998
F Furlanello A Bertoldi M Dallago C Furlanello F Fernando G Inama C Pappone S Chierchia

Arrhythmogenic right ventricular dysplasia (ARVD) is a predisposing factor for sport-related cardiac arrest (CA), sudden cardiac death (SD), and life-threatening ventricular tachyarrhythmias (VT). The aim of this study was the assessment of athletes with ARVD, particularly the CA survivors. From 1974 to January 1996, 1642 competitive athletes (aver. 25.5 yr.), 136 of whom were top level athlete...

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