Results 21 to 30 of about 3,671 (165)

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

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
doaj   +1 more source

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  

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

Long QT Syndrome Type 5 With Coexisting KCNE1 and RYR2 Variants: A Diagnostic Ambiguity

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Long QT syndrome (LQTS) predisposes to syncope and sudden cardiac death. Type 5 LQTS, linked to KCNE1 variants, is rare. A teenage female presented with recurrent syncope. ECG showed QTc 485 ms. Genetic testing identified KCNE1 and RYR2 variants. Beta‐blockers and ICD prevented events.
Mohammad Hossein Nikoo, Hossein Fatemian, Amir Hossein Hassani, Mehrdad Rabiee Rad, Sara Mostafavi   +4 more
wiley   +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

Cardiovascular Health in Women—Across the Lifespan

Clinical Endocrinology, Volume 104, Issue 6, Page 539-555, June 2026.
ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar, Jessica Yao, Simone Gong, Madhuka Wijayarathne, Monique Watts, Swati Mukherjee   +5 more
wiley   +1 more source

Alternative Lead ECG Placements

Annals of Noninvasive Electrocardiology, Volume 31, Issue 3, May 2026.
Alternative ECG lead placements can improve diagnostic yield when the standard 12‐lead ECG is suboptimal or infeasible. This review summarizes practical, scenario‐driven modifications (right‐sided, posterior, seated/prone, Lewis, Fontaine, torso‐based, and monitoring configurations) to better detect ischemia, right ventricular disease/ARVD, and ...
José Luis Morales‐Arteaga, Amin Meghdadi, Derek Wu, Abdullah Bhuiyan, Nicole Langleben, Cengiz Burak, Emily Wilson, Ashley Pellerito, David Aristizábal, Keanu Razzaghi, Juan Maria Farina, Shyla Gupta, Adrian Baranchuk   +12 more
wiley   +1 more source