Results 1 to 10 of about 5,233 (256)

Ebstein Anomaly and Right Aortic Arch in Patient with Charge Syndrome [PDF]

open access: yesMedicina, 2021
Ebstein anomaly is a rare congenital heart disease characterized by a varying degree of anatomical and functional abnormalities of tricuspid valve and right ventricle. It often coexists with other congenital cardiac malformations.
Inguna Lubaua, Madara Teraudkalna
doaj   +5 more sources

Permanent Pacemaker-Mediated Exertional Hypoxemia in a Patient With Ebstein Anomaly [PDF]

open access: goldJACC: Case Reports
Patients with Ebstein anomaly are known to have a higher incidence of interatrial communications and shunting of blood and its components through, mainly due to either streaming of tricuspid regurgitation or due to elevated right atrial pressure. Here we
Ashish H. Shah, MD   +6 more
doaj   +3 more sources

Ebstein Anomaly in Pregnancy [PDF]

open access: yesActa Medica Indonesiana, 2017
A 27-year-old primiparous woman with 28 weeks gestational age was admitted to our hospital with worsening shortness of breath. She was diagnosed with Ebstein’s anomaly three years ago, but preferred to be left untreated. The patient was not cyanotic and
Lusiani Rusdi   +4 more
doaj   +7 more sources

Left ventricular outflow tract obstruction in patients with Ebstein anomalyCentral MessagePerspective [PDF]

open access: yesJTCVS Open, 2023
Objective: In this study, we investigated the clinical characteristics of patients with Ebstein anomaly and left ventricular outflow tract (LVOT) obstruction as well as possible mechanisms of obstruction as assessed by 2-dimensional echocardiography ...
Defne Gunes Ergi, MD   +5 more
doaj   +2 more sources

Displacement of all three leaflets of tricuspid valve: A rare variant of Ebstein anomaly [PDF]

open access: yesClinical Case Reports, 2022
Ebstein anomaly, a rare congenital heart disease, is defined as displacement of hinge points of septal or posterior tricuspid leaflets but not anterior leaflet.
Zahra Khajali   +2 more
doaj   +2 more sources

Successful Radiofrequency Ablation of the Right Lateral Accessory Pathway with Modified Carpentier Reconstruction Surgery in a Patient with Ebstein Anomaly Concomitant of Secundum Atrial Septal Defect, Atrial Fibrillation, and Wolff–Parkinson–White Syndrome [PDF]

open access: goldCase Reports in Vascular Medicine, 2022
Ebstein anomaly (EA) results from the failure of proper delamination of the tricuspid valve leaflets from the right ventricle (RV) myocardium. The severity of EA occurs on a spectrum that results in varying degrees of tricuspid regurgitation, atrial ...
Van Dan Nguyen   +3 more
doaj   +2 more sources

Togetherness of Ebstein anomaly and giant hairy nevus in a neonate: first case in the literature [PDF]

open access: yesThe Turkish Journal of Pediatrics, 2018
Ebstein anomaly is a congenital heart defect in which the septal and posterior leaflets of the tricuspid valve are displaced through the apex of the right ventricle. Giant congenital melanocytic nevi originate from melanocytes.
Ferda Özlü   +5 more
doaj   +3 more sources

Management of Ebstein Anomaly in the Current Era: The Story of One Fetus and the Collaboration of Many—A Case Report [PDF]

open access: yesJournal of Cardiovascular Development and Disease
Collaborative multicenter research has significantly increased our understanding of fetal Ebstein anomaly, delineating risk factors for adverse outcomes as well as predictors of postnatal management.
Ann Kavanaugh-McHugh   +8 more
doaj   +2 more sources

Tricuspid valve septal displacement cutoff value for mortality risk following biventricular repair in Ebstein anomaly [PDF]

open access: yesAnnals of Pediatric Cardiology
Background: Surgical intervention is the definitive treatment for Ebstein anomaly, offering both biventricular and nonbiventricular repair options.
Dicky Fakhri   +6 more
doaj   +2 more sources

Percutaneous PFO closure in adult patient with Ebstein anomaly and cyanosis

open access: goldInternational Journal of Cardiology Congenital Heart Disease, 2021
Ebstein anomaly is a congenital malformation of the tricuspid valve (TV) that is rarely diagnosed in adult population. It is associated with interatrial communication whether by an atrial septal defect (ASD) or parent foramen oval (PFO) in 80–90% of ...
Zahra Nassereddine, MD   +4 more
doaj   +2 more sources

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