Results 51 to 60 of about 3,775 (165)

[Arrhythmogenic right ventricular dysplasia].

Arquivos brasileiros de cardiologia, 1992
To evaluate the clinical findings and complementary investigation to support the diagnosis of arrhythmogenic right ventricular dysplasia.Six males with a mean age of 40 years old with episodes of sustained ventricular tachycardia with left bundle branch block pattern.
I G, Maia, R, Sá, R, Bassan, P, Alves, J C, Ribeiros, L H, Loyola, F E, Cruz Filho, A, Valverde, L, Belém   +8 more
openaire   +2 more sources

Arrhythmogenic Right Ventricular Cardiomyopathy and Cor Triatriatum Dexter: An Unreported Association

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT 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 ...
Erica Franco, Chiara Rovera, Claudio Moretti, Pier Paolo Bassareo   +3 more
wiley   +1 more source

Miocardiopatia arritmogénica do ventrículo direito. Contribuição de diferentes técnicas de eletrocardiografia

Revista Portuguesa de Cardiologia, 2014
Resumo: A miocardiopatia arritmogénica do ventrículo direito – também denominada de displasia arritmogénica do ventrículo direito – é uma patologia em que se verifica a substituição do miocárdio por tecido fibroso ou fibroadiposo predominantemente no ...
Davide Moreira, Anne Delgado, Bruno Marmelo, Emanuel Correia, Pedro Gama, João Pipa, Luís Nunes, Oliveira Santos   +7 more
doaj   +1 more source

Comparing Two‐Dimensional Ellipsoid Model Variants in Estimating Three‐Dimensional Echocardiographic Right Ventricular Volume in Dogs

Journal of Veterinary Internal Medicine, Volume 39, Issue 5, September/October 2025.
ABSTRACT Background Determining right ventricular (RV) volume typically requires three‐dimensional imaging due to its complex shape. The ellipsoid model offers a two‐dimensional alternative, employing area‐ or linear‐based formulas with further variations depending on the echocardiographic views used for measurements.
Robert Ciardullo, Brittany E. Tagg, Elisabeth Nesta, Shana B. Mintz, Romain Pariaut, Weihow Hsue   +5 more
wiley   +1 more source

Right atrial remodelling and prognosis in patients with severe atrial functional tricuspid regurgitation

ESC Heart Failure, Volume 12, Issue 4, Page 2909-2920, August 2025.
Abstract Aims Atrial functional tricuspid regurgitation (AFTR) is increasingly recognized as a distinct cause of tricuspid regurgitation, yet data on outcomes and their determinants are limited. This study examines the prognostic role of right atrial (RA) remodelling in patients with severe AFTR.
Soongu Kwak, Dong‐Jae Han, Seung‐Pyo Lee, Ho Young Hwang, Hyung‐Kwan Kim, Yong‐Jin Kim, Kyung Hwan Kim, Jae Woong Choi, Jun‐Bean Park   +8 more
wiley   +1 more source

A rare presentation of spontaneous ventricular tachycardia in young adult

Heart India, 2017
Arrhythmogenic right ventricular dysplasia (ARVD) is a common cause of sudden cardiac death in young adults. It is a disease that has a wide spectrum of presentation.
Ram Narayan, Mansoor C Abdulla, Jemshad Alungal   +2 more
doaj   +1 more source

Differing impacts of cardiac implantable electronic device leads on tricuspid regurgitation

Journal of Arrhythmia, Volume 41, Issue 4, August 2025.
This study evaluates the impact of different CIED lead types (ICD, RV‐PM, His‐PM) on the progression of tricuspid regurgitation (TR). The effect of CIED leads on TR grade represents a spectrum related to the type of lead traversing the tricuspid valve.
Sophie A. Leon, Melissa Austin, Nayeem Nasher, Daler Rahimov, Faizaan Siddique, Chitra Parikh, Danial Ahmad, Vakhtang Tchantchaleishvili, Behzad B. Pavri   +8 more
wiley   +1 more source

Kocher-Debre-Semelaigne syndrome with arrhythmogenic right ventricular cardiomyopathy: A hitherto unrecognized association

Indian Journal of Endocrinology and Metabolism, 2012
Kocher-Debre-Semelaigne (KDS) syndrome is a rare form of hypothyroid myopathy, with associated hypertrophy of muscles. Although cardiac manifestations of hypothyroidism are well known, reports of cardiac involvement in KDS have only described the ...
Nagaraja Moorthy, Sudeep Kumar, Preeti Dabadghao, Aditya Kapoor   +3 more
doaj   +1 more source

Arrhythmogenic Right Ventricular Cardiomyopathy in Children: A Systematic Review

Diagnostics
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited disease characterized by the progressive replacement of the normal myocardium by fibroadipocytic tissue.
Stefana Maria Moisa, Elena Lia Spoiala, Eliza Cinteza, Radu Vatasescu, Lacramioara Ionela Butnariu, Crischentian Brinza, Alexandru Burlacu   +6 more
doaj   +1 more source

An atypical case report of an arrhythmogenic cardiomyopathy in a 70-years-old patient with suggestive left ventricular signs

Radiology Case Reports
Arrhythmogenic dysplasia of the right ventricule (ARVC), actually known as arrhythmogenic cardiomyopathy (ACM) is a rare genetic condition caused by the replacement of the normal right ventricular myocardium with fibrofatty tissue.
ikram Tahani, MD, oumayma Hattab, MD, Nabila ismaili, PhD, Noha el ouafi, PhD   +3 more
doaj   +1 more source