Results 11 to 20 of about 2,881 (208)

Heterozygous nonsense variants in laminin subunit 3α resulting in Ebstein’s anomaly [PDF]

HGG Advances, 2023
Summary: Ebstein’s anomaly is a rare congenital heart disease characterized by tricuspid valve downward displacement and is associated with additional cardiac phenotypes such as left ventricle non-compaction.
Zhou Zhou, Xumei Huang, Xia Tang, Wen Chen, Qianlong Chen, Chaohui Zhang, Yuxin Li, Dachun Zhao, Zhe Zheng, Shengshou Hu, Jikui Wang, Iftikhar J. Kullo, Keyue Ding   +12 more
doaj   +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   +3 more sources

First Confirmed Case of Leadless Pacemaker Insertion via Bidirectional Glenn Shunt in Ebstein's Anomaly: A Novel Approach to Pacing Challenges. [PDF]

J Cardiovasc Electrophysiol
ABSTRACT Background Ebstein's anomaly presents unique pacing challenges due to complex anatomy and surgical history, often leading to transvenous lead complications. Case Presentation A 28‐year‐old male with Ebstein's anomaly, prior Danielson tricuspid valve repair, and bidirectional Glenn shunt presented with acute ventricular pacing loss from ...
Doyle RS, Temperley HC, Murray C, Walsh K.   +3 more
europepmc   +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

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

An Unusual Case of Tricuspid Stenosis [PDF]

European Journal of Case Reports in Internal Medicine, 2018
Tricuspid stenosis is an uncommon valvular abnormality commonly associated with other valvular lesions. Ebstein's anomaly is a rare congenital heart malformation characterized primarily by abnormalities of the tricuspid valve and right ventricle ...
Sara Ferreira, Arsénio Barbosa, Filipa Gomes, Jorge Almeida, Jorge Santos Almeida, Mário Amorim, José Paulo Araújo   +6 more
doaj   +4 more sources

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

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

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

Rare loss-of-function variants in matrisome genes are enriched in Ebstein’s anomaly [PDF]

HGG Advances
Summary: Ebstein’s anomaly, a rare congenital heart disease, is distinguished by the failure of embryological delamination of the tricuspid valve leaflets from the underlying primitive right ventricle myocardium. Gaining insight into the genetic basis of
Zhou Zhou, Xia Tang, Wen Chen, Qianlong Chen, Bo Ye, Angad S. Johar, Iftikhar J. Kullo, Keyue Ding   +7 more
doaj   +2 more sources

Dichorionic-Diamniotic Twin Pregnancy in a Bicornuate Uterus With Twin A Affected by Ebstein's Anomaly. [PDF]

Cureus, 2023
Congenital Mullerian anomalies are rare developmental defects that result in malformation of the fallopian tubes, uterus, cervix, and vagina. The bicornuate uterus is one of the many variants of Mullerian anomalies, defined as having an external fundal ...
Gorman CN, Grabois SA, Mathur S, Grabois EP, Silanee A.   +4 more
europepmc   +3 more sources