Results 11 to 20 of about 3,775 (165)

Arrhythmogenic Right Ventricular Dysplasia [PDF]

open access: yesCirculation, 2005
Background— Arrhythmogenic right ventricular dysplasia (ARVD) is an inherited cardiomyopathy characterized by right ventricular dysfunction and ventricular arrhythmias.
Darshan, Dalal   +14 more
  +8 more sources

Arrhythmogenic right ventricular dysplasia. [PDF]

open access: yesHeart, 1993
Arrhythmogenic right ventricular dysplasia is a relatively newly described clinical entity that is more and more frequently recognized. It may explain an increasing number of unexpected, sudden deaths in young adults that are or are not preceded by cardiac symptoms. A genetic transmission of the disease has been suggested by the study of familial cases.
openaire   +4 more sources

Physical exercise and arrhythmogenic right ventricular cardiomyopathy/dysplasia: An overview

open access: yesHeart Views, 2022
Arrhythmogenic right ventricular cardiomyopathy/dysplasia is inherited cardiomyopathy that has a propensity for ventricular arrhythmia, ventricular dysfunction, and sudden cardiac death.
Rasha Kaddoura, Hassan Al-Tamimi
doaj   +1 more source

Long Term Follow-Up in a Patient with Arrhythmogenic Right Ventricular Dysplasia [PDF]

open access: yesRomanian Journal of Cardiology, 2021
This case report describes eight years of follow-up in a young adult with arrhythmogenic right ventricular dysplasia (ARVD). He presented with exertional palpitations, symmetric T wave inversions and possible epsilon waves in the right precordial leads ...
Diana-Aurora BORDEJEVIC   +8 more
doaj   +1 more source

Arrhythmogenic Right Ventricular Dysplasia

open access: yesCurrent Problems in Cardiology, 2013
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD) is a genetic cardiomyopathy characterized by ventricular arrhythmias and structural abnormalities of the right ventricle (RV). The discovery of desmosomal mutations associated with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) has led researchers to hypothesize equal ...
Romina L. Caprini, José L. Cacharron
  +6 more sources

Management of a rare case of arrhythmogenic right ventricular dysplasia in pregnancy: a case report

open access: yesJournal of Medical Case Reports, 2011
Introduction Arrhythmogenic right ventricular dysplasia is a heritable disease of the heart muscle characterized by fibrofatty degeneration of cardiomyocytes. Patients present with ventricular arrhythmias or congestive heart failure, and sometimes sudden
İşçi Herman   +5 more
doaj   +1 more source

Left Ventricular Dysfunction in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC): Can We Separate ARVC From Other Arrhythmogenic Cardiomyopathies?

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2020
Arrhythmogenic right ventricular cardiomyopathy was first described as a right ventricular disease that is an important cause of death in young adults. However, with the advent of advanced imaging, arrhythmogenic right ventricular cardiomyopathy has been
Stephan Altmayer   +2 more
doaj   +1 more source

An induced pluripotent stem cell line (EHTJUi004-A) generated from a neonate with c.4683_4684delCT:p.Leu1563fs mutation in the gene DSP causing Familial Arrhythmogenic Right Ventricular Dysplasia (ARVD)

open access: yesStem Cell Research, 2021
Familial Arrhythmogenic Right Ventricular Dysplasia (ARVD) is a primary cardiomyopathy characterized by the abnormality of the right ventricular muscle. ARVD may be life-threatening due to the induction of paroxysmal refractory ventricular tachycardia or
Yi-Yao Qi   +9 more
doaj   +1 more source

Catheter Ablation of Ventricular Tachycardia in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: A Sequential Approach

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2019
Background It has been suggested that endocardial and epicardial ablation of ventricular tachycardia (VT) improves outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Shibu Mathew   +18 more
doaj   +1 more source

A case of arrhythmogenic right ventricular dysplasia/cardiomyopathy with pneumothorax and degloving injury of the right upper limb

open access: yesBLDE University Journal of Health Sciences, 2020
Arrhythmogenic right ventricular dysplasia / cardiomyopathy (ARVD / C) is a rare genetic cardiomyopathy characterized by fibro-fatty replacement primarily of the right ventricular myocytes,and can present as any of 'concealed' disease, 'overt arrhythmia'
Varun Suresh
doaj   +1 more source

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