Results 21 to 30 of about 3,775 (165)

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, Ichiro Watanabe, Yasuo Okumura, Kazumasa Sonoda, Koichi Nagashima, Toshiko Nakai, Kimie Ohkubo, Tatsuya Kofune, Hironori Haruta, Masayoshi Kofune, Satoshi Kunimoto, Atsushi Hirayama   +11 more
doaj   +1 more source

Evolution of diagnostic criteria for arrhythmogenic right ventricular cardiomyopathy and their application in clinical practice

Российский кардиологический журнал, 2021
This article describes evolution of criteria for arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). The novel diagnostic criteria for ARVD/C published in 2020 are analyzed in detail, among which biventricular and leftdominant ...
Yu. A. Lutokhina, O. B. Blagova, A. G. Shestak, E. V. Zaklyazminskaya, S. A. Alexandrova, A. V. Nedostup   +5 more
doaj   +1 more source

Treatment of arrhythmogenic right ventricular cardiomyopathy (dysplasia) [PDF]

Кардіохірургія та інтервенційна кардіологія, 2016
Arrhythmogenic right ventricular cardiomyopathy (dysplasia) is an inheritable heart muscle disease predisposing to ventricular arrhythmias and increasing risk of sudden cardiac death.
M.Т. Vatutin, G.S. Smyrnova, Y.V. Yeshchenko, G.E. Degtiarova, V.S. Kolesnikov, Y.P. Gritsenko   +5 more
doaj  

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
openaire   +2 more sources

First Reported Case of Arrhythmogenic Right Ventricular Cardiomyopathy in Oman

Oman Medical Journal, 2017
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare genetic disorder characterized by fatty degeneration of the right ventricular myocardium with variable involvement of the left ventricle.
Hatim Al Lawati, Humoud Al Dhuhli
doaj   +1 more source

Electrocardiographic Patterns of Ventricular Arrhythmias in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Frontiers in Physiology, 2012
Ventricular arrhythmias in patients with ARVD/C are common. Differentiation between idiopathic ventricular tachycardia and arrhythmogenic right ventricular dysplasia is of utmost importance.
Kurt eHoffmayer, Melvin M Scheinman
doaj   +1 more source

Arrhythmogenic Cardiomyopathy

Zdravniški Vestnik, 2019
Arrhythmogenic cardiomyopathy (AC) is a genetic disease of the myocardium characterized by fibro-fatty replacement of the apoptotic myocardium. It primarily affects the right ventricle, however in advanced stages of the disease the left ventricle can ...
Blaž Podgoršek, Gregor Poglajen, Andraž Cerar, Matjaž Šinkovec, Bojan Vrtovec   +4 more
doaj   +1 more source

Patent Foramen Ovale: Epidemiology, Risk Factors, Pathophysiology, Clinical Features, Diagnosis, and Management

MedComm, Volume 7, Issue 9, September 2026.
The clinical manifestations of PFO. Although the majority of PFOs are benign and asymptomatic, they can present with a variety of clinical manifestations, or coexisting with other diseases and aggravating their symptoms, including cerebral diseases (such as CS, epilepsy, TIA, or migraine), systemic embolism (such as embolism in renal artery, coronary ...
Linlin Meng, Xiaotong Zhang, Guangrui Sun, Honggang Dai, Xiao Meng, Cheng Zhang, Yun Zhang   +6 more
wiley   +1 more source

Prenatally diagnosed cleft lip and palate: Prenatal findings, clinical outcomes, genetic results, and sequencing yield in isolated versus non‐isolated cases

Pregnancy, Volume 2, Issue 5, September 2026.
Abstract Introduction Cleft lip and palate (CLP) are common congenital disruptions of the orofacial cleft and are associated with numerous genetic conditions. This study examines prenatal findings, clinical outcomes, and genetic findings among prenatally diagnosed CLP, with a focus on the yield of next‐generation sequencing (NGS).
Thomas P. Kishkovich, Gabriela F. Tessler, Meghan Angley, Yijia Zhang, Thomas A. Imahiyerobo, Sherelle L. Laifer‐Narin, Hong Ma, Lynn Simpson, Caitlin D. Baptiste, Jessica L. Giordano, Russell S. Miller, Ronald J. Wapner   +11 more
wiley   +1 more source

Catheter Ablation in Arrhythmic Cardiac Diseases: Endocardial and Epicardial Ablation

Reviews in Cardiovascular Medicine, 2022
Arrhythmogenic cardiomyopathy (ACM) is a group of arrhythmogenic disorders of the myocardium that are not caused by ischemic, hypertensive, or valvular heart disease.
Wen-Han Cheng, Fa-Po Chung, Yenn-Jiang Lin, Li-Wei Lo, Shih-Lin Chang, Yu-Feng Hu, Ta-Chuan Tuan, Tze-Fan Chao, Jo-Nan Liao, Chin-Yu Lin, Ting-Yung Chang, Ling Kuo, Cheng-I Wu, Chih-Min Liu, Shin-Huei Liu, Shih-Ann Chen   +15 more
doaj   +1 more source