Results 31 to 40 of about 4,606 (191)
Long Term Follow-Up in a Patient with Arrhythmogenic Right Ventricular Dysplasia [PDF]
Romanian 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
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Arrhythmogenic right ventricular dysplasia. [PDF]
Heart, 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.
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Management of a rare case of arrhythmogenic right ventricular dysplasia in pregnancy: a case report
Journal 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
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Journal 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
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Stem 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
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Journal 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
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BLDE 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
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Arrhythmogenic Right Ventricular Cardiomyopathy and Cor Triatriatum Dexter: An Unreported Association. [PDF]
Clin Case RepABSTRACT We present a 74‐year‐old patient with a previous diagnosis of arrhythmogenic right ventricular cardiomyopathy manifesting as heart failure where a concomitant cor triatriatum dexter has accidentally been diagnosed by echocardiography. The association between arrhythmogenic right ventricular cardiomyopathy and cor triatriatum dexter has not ...
Franco E +3 more
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Arrhythmogenic right ventricular dysplasia
The American Journal of Emergency Medicine, 2001 Right ventricular dysplasia (RVD) is a disease entity of unknown cause that is characterised by partial or total replacement of RV-muscle by adipose or fibrous tissue. It is a well-recognized cause of arrhythmia and premature sudden death, but usually underdiagnosed.
A J, Kinsara, L, Zaman, A, Gorgels
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Atrial tachycardia in a patient with arrhythmogenic right ventricular cardiomyopathy/dysplasia
Journal of Arrhythmia, 2013 We describe a 49-year-old woman with atrial tachycardia (AT) and arrhythmogenic right ventricular cardiomyopathy/dysplasia. Cardiac magnetic resonance images showed a markedly dilated right atrium and right ventricle.
Hiroaki Mano +11 more
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