Results 51 to 60 of about 200,194 (156)
Ebstein’s Anomaly: Anesthetic Management at shahid Gangalal National Heart Centre
, 2017 During the last eight years, 34% of the cases have been congenital; out of which only 0.7% have been Ebstein’s Anomaly. In the literature they have mentioned that the male and female ratio is 1:1, but there are more female than male in our series, 15:3.
Jeju Nath Pokharel, Murari Raj Upreti
core +1 more source
Antenatal Imaging of Ebstein’s Anomaly with Hydrops Fetalis
Medical Journal of Dr. D.Y. Patil VidyapeethEbstein’s anomaly is a rare congenital cardiac anomaly characterized by tricuspid valve (TV) malformation, including the low insertion of the septal and posterior leaflets of the TV into the tricuspid annulus. It is one of the common malformations of the
Shrishail Adke +2 more
doaj +1 more source
Ebstein’s anomaly treated surgically in an adult female [PDF]
, 2016 A 21-year-old woman with Ebstein’s anomaly was admitted with syncope on exertion, fatigue and dyspnea (NYHA III). Physical examination revealed systolic apical murmur.
Frączek-Jucha, Magdalena Maria; Department of Coronary Disease and Heart Failure, Jagiellonian University Medical College, John Paul II Hospital, Krakow, Poland +6 more
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Journal of Pediatric Gastroenterology and Nutrition, Volume 83, Issue 4, Page 737-743, October 2026.Abstract Objectives Malnutrition in patients with critical congenital heart disease (CCHD) is associated with worse outcomes, however, feeding challenges, and changes in metabolic demands obscure the relationship between nutrient intake and growth in this patient population.
Colin R. Tang‐Whitmore +8 more
wiley +1 more source
Acta Médica Portuguesa, 1994 Ebstein's Anomaly of the tricuspid valve has a variable degree of abnormality with a continuous change between mild and severe forms and, consequently, a variable clinical course. Pregnancy can also be well tolerated with a good fetal outcome.
J M Santos +5 more
doaj +1 more source
American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 2099-2105, September 2026.ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide +10 more
wiley +1 more source
Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects
American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 1953-1972, September 2026.ABSTRACT Cases with congenital heart defects (CHD) often have other associated anomalies. The aim of this investigation was to assess the prevalence and the types of co‐occurring anomalies in CHD in a well‐defined population. The anomalies co‐occurring with CHD were ascertained in all live births, stillbirths and terminations of pregnancy for fetal ...
Claude Stoll +2 more
wiley +1 more source
British Journal of Clinical Pharmacology, Volume 92, Issue 9, Page 3037-3048, September 2026.Abstract Aim Besides registries, healthcare databases can provide useful information for assessing the frequency of major congenital malformations (MCMs) and investigating their risk factors, particularly medication exposures. This study aimed to assess the validity of MCMs identification based on French national, comprehensive healthcare databases ...
Tom Duchemin +7 more
wiley +1 more source
Pregnancy, Volume 2, Issue 5, September 2026.Abstract Introduction Pregnant people with congenital heart disease (CHD) are a growing patient population in obstetrics, yet evidence on the risk for severe maternal morbidity (SMM) has largely been limited to studies that lack specificity for CHD. We conducted this study to demonstrate the utility of distributed data networks for obstetric research ...
Elizabeth B. Sherwin +11 more
wiley +1 more source