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1 Ebstein anomaly and tricuspid valve dysplasia are rare c
2 Ebstein anomaly is a spectrum of tricuspid valvular and
3 Ebstein anomaly is the most common cause of primary tric
4 Ebstein's anomaly and other tricuspid valve abnormalitie
5 Ebstein's anomaly was diagnosed in one lithium-exposed f
6 Ebstein's malformation coexisted in 18 patients.
7 25%), tricuspid atresia (12 patients, 20%), Ebstein's anomaly (4 patients, 6.5%), pulmonic atresia o
8 trial to right ventricle bioprosthesis in 3, Ebstein's anomaly of the TV in 5, and other in 6), and 2
10 dum atrial septal defect (ASD) (n = 71), and Ebstein's malformation (n = 7) for NKX2.5 mutations.
12 ter category encompasses CHD lesions such as Ebstein anomaly, transposition of the great arteries wit
15 irst report of individuals being affected by Ebstein anomaly because of a mutation in this gene and d
16 adults with congenital heart disease (CHD): Ebstein's anomaly, the failing Fontan, and pulmonary val
17 , including atrioventricular septal defects, Ebstein malformation of the tricuspid valve, and perimem
20 tricular septal defect, tetralogy of Fallot, Ebstein anomaly, transposition of the great vessels, and
25 performed on adults with CHD are surgery for Ebstein's anomaly, Fontan revision, and pulmonary valve
26 mmunosuppression with anti-viral therapy for Ebstein-Barr virus (EBV) is the primary treatment for al
29 l dysfunction is a predictor of mortality in Ebstein anomaly, and RA dysfunction and hypertension are
30 the use of RVGLS for risk stratification in Ebstein anomaly, and further studies are required to ass
32 with the emergence of severe CHDs including Ebstein's anomaly, atrioventricular septal defect, and o
33 sed risk of cardiac malformations, including Ebstein's anomaly; the magnitude of this effect was smal
35 ciated with a marked increase in the risk of Ebstein's anomaly (a right ventricular outflow tract obs
38 rofound cardiogenic shock caused by a severe Ebstein anomaly can be successfully salvaged with fenest
40 a mean age of 26+/-14 years with unrepaired Ebstein anomaly were examined in a prospective study.
41 The most frequent cardiac diagnoses were Ebstein's anomaly (40%), pulmonary atresia (11%), and te
43 ts at the Mayo Clinic from 1987 to 2020 with Ebstein anomaly and CIED procedure were reviewed for pro
45 his was a retrospective study of adults with Ebstein anomaly who received care at Mayo Clinic from 20
47 ce of LV fibrosis replacement in adults with Ebstein anomaly, characterized by specific CMR and histo
53 s large, contemporary series of fetuses with Ebstein anomaly and tricuspid valve dysplasia, perinatal
54 e with severe tetralogy of Fallot, four with Ebstein's anomaly and two with single ventricle and pulm
55 electronic devices (CIEDs) in patients with Ebstein anomaly during tricuspid valve (TV) surgery is u
58 1972, to January 1, 2006, 539 patients with Ebstein anomaly underwent 604 cardiac operations at the
59 ong-term functional outcome of patients with Ebstein anomaly who had cardiac operation at our institu