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 +4 more
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Circulation, 1957 Four cases of Ebstein's anomaly are described, revealing that the clinical features permit diagnosis in the majority of instances and that cardiac catheterization affords precise confirmation of the diagnosis. The occurrence of this anomaly in acyanotic adults is pointed out, and the similarity to acquired valvular rheumatic heart disease is stressed.
S G, BLOUNT, I J, GELB, M C, MCCORD
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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 +12 more
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Case report of Ebstein’s anomaly in a young female [PDF]
SAGE Open Medical Case ReportsEbstein’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 +3 more
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Cardiovascular magnetic resonance evidence of myocardial fibrosis and its clinical significance in adolescent and adult patients with Ebstein’s anomaly [PDF]
Journal of Cardiovascular Magnetic Resonance, 2018 Background Myocardial fibrosis is a common pathophysiological process that is related to ventricular remodeling in congenital heart disease. However, the presence, characteristics, and clinical significance of myocardial fibrosis in Ebstein’s anomaly ...
Dan Yang +12 more
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Effective Pharmacotherapy, 2022 Ebstein’s anomaly is a rare congenital malformation characterized by apical displacement of the right atrioventricular ring with an anomaly of the development of the tricuspid valve and the frequent presence of other heart defects. According to our data, this defect was diagnosed in 2 cases in more than 6 000 sectional studies: in an adult and a child.
V.M. Delyagin +2 more
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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 DiseaseBackground 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 +4 more
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Intraoperative Hemodynamic Instability in a Patient With Ebstein’s Anomaly Complicated With Eisenmenger Syndrome [PDF]
Case Reports in CardiologyEbstein’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 +4 more
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Rare loss-of-function variants in matrisome genes are enriched in Ebstein’s anomaly [PDF]
HGG AdvancesSummary: 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 +7 more
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Novel Case of Prader-Willi Syndrome and Ebstein's Anomaly: Implications for Complex Care Management. [PDF]
J Pediatr Genet, 2022 Mattia D +4 more
europepmc +3 more sources