نتایج جستجو برای: arvd

تعداد نتایج: 232  

Journal: :Heart 2002
F Niroomand C Carbucicchio C Tondo S Riva G Fassini A Apostolo 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...

Journal: :Circulation 2011
Moniek G P J Cox Paul A van der Zwaag Christian van der Werf Jasper J van der Smagt Maartje Noorman Zahir A Bhuiyan Ans C P Wiesfeld Paul G A Volders Irene M van Langen Douwe E Atsma Dennis Dooijes Arthur van den Wijngaard Arjan C Houweling Jan D H Jongbloed Luc Jordaens Maarten J Cramer Pieter A Doevendans Jacques M T de Bakker Arthur A M Wilde J Peter van Tintelen Richard N W Hauer

BACKGROUND Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an autosomal dominant inherited disease with incomplete penetrance and variable expression. Causative mutations in genes encoding 5 desmosomal proteins are found in ≈50% of ARVD/C index patients. Previous genotype-phenotype relation studies involved mainly overt ARVD/C index patients, so follow-up data on relatives...

Journal: :Circulation. Cardiovascular genetics 2009
A Dénise den Haan Boon Yew Tan Michelle N Zikusoka Laura Ibañez Lladó Rahul Jain Amy Daly Crystal Tichnell Cynthia James Nuria Amat-Alarcon Theodore Abraham Stuart D Russell David A Bluemke Hugh Calkins Darshan Dalal Daniel P Judge

BACKGROUND Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited disorder typically caused by mutations in components of the cardiac desmosome. The prevalence and significance of desmosome mutations among patients with ARVD/C in North America have not been described previously. We report comprehensive desmosome genetic analysis for 100 North Americans with clinicall...

2017
Fa-Po Chung Yenn-Jiang Lin Ling Kuo Shih-Ann Chen

Differentiating arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) from other cardiomyopathies is clinically important but challenging. Although the modified Task Force Criteria can facilitate diagnosis of ARVD/C according to clinical manifestations, histopathological examination plays a pivotal role in excluding other diseases that can mimic ARVD/C. Here, we report a patient wi...

2014
Soraya El Ghannudi Anthony Nghiem Philippe Germain Mi-Young Jeung Afshin Gangi Catherine Roy

BACKGROUND Few studies evaluated left ventricular (LV) involvement in arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). The aim of this study is to determine the frequency, clinical presentation, and pattern of LV involvement in ARVD/C (LV-ARVD/C). METHODS We retrospectively evaluated the cardiac magnetic resonance (CMR) in 202 patients referred between 2008 and 2012 to our ...

Journal: :Journal of the American College of Cardiology 2011
Hugh Calkins

Arrhythmogenic right ventricular dysplasia (ARVD) is an inherited cardiomyopathy that is characterized by ventricular arrhythmias, an increased risk of sudden death, and abnormalities of right ventricular (RV) structure and function. The pathological hallmark of ARVD is myocyte loss with fibro-fatty replacement. Since the first detailed clinical description of the disorder in 1982, significant ...

Journal: :Circulation. Arrhythmia and electrophysiology 2010
Moniek G P J Cox Jasper J van der Smagt Maartje Noorman Ans C Wiesfeld Paul G A Volders Irene M van Langen Douwe E Atsma Dennis Dooijes Arjan C Houweling Peter Loh Luc Jordaens Yvonne Arens Maarten J Cramer Pieter A Doevendans J Peter van Tintelen Arthur A M Wilde Richard N W Hauer

BACKGROUND Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) Diagnostic Task Force Criteria (TFC) proposed in 1994 are highly specific but lack sensitivity. A new international task force modified criteria to improve diagnostic yield. A comparison of diagnosis by 1994 TFC versus newly proposed criteria in 3 patient groups was conducted. METHODS AND RESULTS In new TFC, scoring...

Journal: :Circulation 2009
Rahul Jain Darshan Dalal Amy Daly Crystal Tichnell Cynthia James Ariana Evenson Rohit Jain Theodore Abraham Boon Yew Tan Hari Tandri Stuart D Russell Daniel Judge Hugh Calkins

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 ...

Journal: :Circulation. Arrhythmia and electrophysiology 2012
Haris M Haqqani Cory M Tschabrunn Brian P Betensky Nimrod Lavi Wendy S Tzou Erica S Zado Francis E Marchlinski

BACKGROUND Ventricular tachycardia ablation in arrhythmogenic right ventricular dysplasia (ARVD) is more successful when including epicardial ablation. Scarring may cause independent, layered epicardial activation and promote epicardially confined ventricular tachycardia circuits. We aimed to characterize transmural right ventricular activation in ARVD patients and to compare this with referenc...

Journal: :Journal of Cardiovascular Magnetic Resonance 2008
Aditya Jain Harikrishna Tandri Hugh Calkins David A Bluemke

Arrhythmogenic right ventricular dysplasia (ARVD) is a genetic cardiomyopathy characterized clinically by ventricular arrhythmias and progressive right ventricular (RV) dysfunction. The histopathologic hallmark is fibro-fatty replacement of RV myocardium. It is inherited in an autosomal pattern with variable penetrance. ARVD is unique in that it most commonly presents in young, otherwise health...

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