Results 31 to 40 of about 5,762 (257)

Ebstein′s anomaly with severe aortic stenosis and syncope: Implications in management

Sahel Medical Journal, 2013
Ebstein′s anomaly is a rare congenital heart disease involving the right side of the heart with typical malformations of the tricuspid valve and the right ventricle.
Vijayakumar Subban, Anitha Lakshmanan, Latchumanadhas Kalidoss, Ulhas M Pandurangi, Ajit S Mullasari   +4 more
doaj   +1 more source

Prognostic role and hemodynamic mechanism of impaired aerobic capacity in adults with Ebstein anomaly

International Journal of Cardiology Congenital Heart Disease, 2021
Background: Patients with Ebstein anomaly have impaired aerobic capacity, but the relationship between aerobic capacity and clinical outcomes are unknown.
Alexander C. Egbe, William R. Miranda, Joseph A. Dearani, Renuka R. Katta, Ahmed Y. Goda, Momina Iftikhar, Heidi M. Connolly   +6 more
doaj   +1 more source

Image to Fit the Clinical Picture: Point-of-care Ultrasound Assessment of Ebstein’s Anomaly in Peru [PDF]

, 2020
Ebstein’s anomaly is a congenital heart defect that when left untreated can lead to unique physical exam and ultrasound findings. This case describes a patient who presented with dyspnea and was found to have cyanosis, clubbing, and dilation of right ...
Dreyfuss, Andrea, Inga, Roberto, Rider, Ashley C.   +2 more
core  

Pediatric Giant Right Atrial Aneurysm: A Case Series and Review of the Literature [PDF]

, 2013
Giant right atrial aneurysm is a rare form of congenital heart disease with a wide spectrum of clinical presentation varying from asymptomatic patients to those with refractory atrial arrhythmias or severe airway obstruction.
Harder, Erika E., Knepp, Marc D., Ohye, Richard G., Owens, Sonal T.   +3 more
core   +1 more source

Percutaneous PFO closure in adult patient with Ebstein anomaly and cyanosis

International 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, Fida Charif, MD, Claudette Najjar, MD, Dani Youssef, MD, Mohamad Saab, MD   +4 more
doaj   +1 more source

A dual-chamber leadless pacemaker implantation across percutaneous tricuspid valve-in-valve prosthesis in a patient with Ebstein anomaly. [PDF]

HeartRhythm Case Rep
Al-Ghamdi BS, Salem MD, Echahidi MN.
europepmc   +3 more sources

Mapping of accessory pathways in pediatric patients with Ebstein anomaly using open-window mapping. [PDF]

HeartRhythm Case Rep
Ezzeddine FM, Amin H, Cannon B.
europepmc   +3 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

Case 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, Xuan Tuan Nguyen, Van Tung Pham, Le Tra Pham   +3 more
doaj   +1 more source

Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7 [PDF]

, 2011
Ebstein's anomaly is a rare congenital heart malformation characterised by adherence of the septal and posterior leaflets of the tricuspid valve to the underlying myocardium.
A. F. M. Moorman, A. T. J. M. Helderman-van den Enden, A. V. Postma, B. J. M. Mulder, B. Keavney, H. W. Vliegen, J-W Sels, J. B. A. van de Meerakker, J. Goodship, J. W. Roos-Hesselink, K. van Engelen, M. J. H. Baars, S. Klaassen, S. R. Sperling, T. Pickardt, T. Rahman, U. Bauer   +16 more
core   +1 more source

Impact of Isolated Tricuspid Valve Repair on Right Ventricular Remodelling in an Adult Congenital Heart Disease Population [PDF]

, 2017
BackgroundSurgical repair of isolated congenital tricuspid valve (TV) disease is rare with no well-defined indication and outcomes. Moreover, the role of right ventricle (RV) in this context has not yet been investigated.ObjectivesWe sought to assess the
Baritussio, Anna, Benedetto, Umberto, Bruno, Vito, Caputo, Massimo, Chivasso, Pierpaolo, Guida, Gustavo, Marsico, Roberto, Rapetto, Filippo   +7 more
core   +3 more sources