Results 11 to 20 of about 239,154 (181)

Simultaneous Heart–Kidney Transplantation for Ebstein's Anomaly: A Viable Treatment Option in Latin America [PDF]

Clinical Case Reports, Volume 14, Issue 8, August 2026.
Chest x‐ray showing a typical presentation of Ebstein anomaly with severe cardiomegaly and a prominent right atrium silhouette. ABSTRACT Simultaneous heart–kidney transplantation is a viable and effective treatment option for patients with congenital heart disease and advanced chronic kidney disease when both conditions threaten survival.
Edgar García‐Cruz, Andrea Luna‐Hernández, Jesús Alberto Blanco‐Hernández, Jorge Sánchez‐Nieto, Stephanie Teresa Angulo‐Cruzado, Karla Alejandra Pupiales‐Dávila, Carla Domínguez‐Pereyra, Reyna Moreno‐Ruíz, Carlos Antonio Villegas‐Chávez, Antonio Jordán‐Ríos, Daniel Manzur‐Sandoval, Victor Alejandro Quiroz‐Martínez, Francisco Martín Baranda‐Tovar   +12 more
wiley   +2 more sources

Atrial septal defect device closure and concurrent atrio‐fascicular Mahaim ablation in adult patient with Ebstein's anomaly

Clinical Case Reports, 2022
Ebstein's anomaly is an uncommon congenital malformation which might be associated with atrial septal defect and atrio‐fascicular Mahaim. Here, we report a known case of Ebstein's anomaly with atrial septal defect and concomitant atrio‐fascicular Mahaim ...
Zahra Khajali, Atta Firouzi, Masoud Farzad Kabir, Iman Harirforoosh, Maryam Aliramezany   +4 more
doaj   +2 more sources

Quantification of Tricuspid Valve Regurgitation With 2D and 4D‐Flow MRI: Comparison of Different Methods in Adult Patients With Ebstein's Anomaly [PDF]

Journal of Magnetic Resonance Imaging, Volume 64, Issue 2, Page 515-523, August 2026.
ABSTRACT Background Ebstein's anomaly (EA) is a congenital heart disorder involving tricuspid valve dysplasia and right heart abnormalities resulting in severe tricuspid regurgitation (TR). Multiple techniques assess regurgitation severity, but their correlation with EA severity markers remains unclear. Purpose To compare MRI techniques for quantifying
Eric Buffle, Mathieu Albertini, Damian Craiem, Victor Waldmann, Francesca Pitocco, Laurence Iserin, Umit Gencer, Elie Mousseaux, Gilles Soulat   +8 more
wiley   +2 more sources

First description of combined Ebstein's anomaly and quadricuspid aortic valve [PDF]

Eur Heart J Case Rep
Meier C, Rubesch-Kütemeyer V, Pula A, Gielen S. First description of combined Ebstein's anomaly and quadricuspid aortic valve. European Heart Journal - Case Reports .
Gielen, Stephan, Rubesch-Kütemeyer, Vanessa, Meier, Claudia, Pula, Arianit   +3 more
core   +2 more sources

Postpartum Deterioration of Hemodynamics in a Case of Uncorrected Ebstein's Anomaly [PDF]

Case Reports in Cardiology, 2012
Ebstein's anomaly is a rare congenital cardiac malformation that is characterized by abnormalities of the tricuspid valve and right ventricle. Pregnancy is usually well tolerated unless cyanosis or arrhythmia develops.
Masato Kimura, Shuhei Kakizaki, Seiichi Tazawa, Osamu Adachi, Yoshikatsu Saiki, Shigeo Kure   +5 more
doaj   +2 more sources

Fetal Conduction Disease and Arrhythmia in Ebstein's Anomaly and Tricuspid Valve Dysplasia Assessed by Fetal Magnetocardiography [PDF]

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Ebstein's anomaly and tricuspid valve dysplasia are associated with perinatal mortality approaching 50% and are among the most difficult fetal conditions to manage.
Annette Wacker‐Gussmann, Gabriela Tardelli, Bettina F. Cuneo, Janette F. Strasburger, Ronald T. Wakai   +4 more
doaj   +2 more sources

Case report of Ebstein’s anomaly in a young female [PDF]

SAGE Open Medical Case Reports
Ebstein’s anomaly, also known as Ebstein’s malformation, is a congenital heart defect that occurs in about 0.005% of live births and accounts for 0.3–0.6% of all congenital heart disease.
Rediet Dessalegne, Yoseph Bekele, Selamawit Getachew, Mekdelawit Birhanu   +3 more
doaj   +2 more sources

Intraoperative Hemodynamic Instability in a Patient With Ebstein’s Anomaly Complicated With Eisenmenger Syndrome [PDF]

Case Reports in Cardiology
Ebstein’s anomaly is a rare congenital displacement of the tricuspid valve resulting in atrialization of the right ventricle. About half of the patients with Ebstein’s anomaly also have atrial septal defects, which may lead to chronic shunting and ...
Leonardo A. Marquez Roa, Jorge Araujo-Duran, Richard Hofstra, Jibran Ikram, Sabry Ayad   +4 more
doaj   +2 more sources

Ebstein's Anomaly: Genetics, Clinical Manifestations, and Management

Pediatrics and Neonatology, 2017
Ebstein's anomaly is uncommon. Genetic bases of this congenital heart defect may be related to the mutations in myosin heavy chain 7 and NKX2.5, among others. Asymptomatic patients with Ebstein's anomaly can be conservatively treated and kept under close
Shi-Min Yuan
doaj   +2 more sources

Lithium-induced Ebstein’s Anomaly

Heart Views
Ebstein’s anomaly (EA) is a rare congenital cardiac defect that occurs when the tricuspid valve leaflets fail to delaminate from the ventricular myocardium, they adhere to the underlying myocardium. Multiple etiologies such as genetic mutation in NKX2-5,
Vijaykumar Gupta, Priyavardhan Mishra, Priyanka Mirdha, Anant Patil   +3 more
doaj   +2 more sources