Results 11 to 20 of about 7,984 (209)
Arrhythmogenic right ventricular dysplasia [PDF]
Australian and New Zealand Journal of Medicine, 1991 Abstract A 23‐year‐old man presented with recurrent exercise‐induced ventricular tachycardia (VT), complicated by systemic embolisation. Catecholamine ‐ sensitive VT was reproduced on exercise testing and programmed electrical stimulation, displaying features suggestive of enhanced automaticity as well as re‐entry.
D, Fatkin +3 more
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From Palpitations to Prevention: Timely Recognition of Biventricular ACM Preventing Sudden Cardiac Death. [PDF]
Case Rep CardiolSudden cardiac death (SCD) is a prevalent and significant health concern which may be preceded by palpitations and presyncope in a young patient. Of the arrhythmogenic causes of SCD, arrhythmogenic cardiomyopathy (ACM) is rare but important with a high morbidity and mortality.
Singh J, Adel FW, Chen HH.
europepmc +2 more sources
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy [PDF]
Circulation, 2003 Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a disease characterized by fatty replacement of the right ventricular muscle (1). The residual myocardial fibers are often embedded in fibrous tissue. This substrate is conducive to right ventricular re-entrant arrhythmias. Initially this condition was called dysplasia because it was
Kathleen, Gear, Frank, Marcus
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Physical exercise and arrhythmogenic right ventricular cardiomyopathy/dysplasia: An overview
Heart 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
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Arrhythmogenic Right Ventricular Dysplasia
Current 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 ...
Wojciech Mazur +3 more
+6 more sources
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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