Results 81 to 90 of about 439,883 (208)

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, Yves Alembik, Marie‐Paule Roth   +2 more
wiley   +1 more source

Identification of major congenital malformations based on healthcare databases in France: A proof‐of‐concept study using the epi‐meres nationwide mother–child register

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, Lise Marty, Jérôme Drouin, Sara Miranda, Jérémie Botton, Valérie Olié, Alain Weill, Rosemary Dray‐Spira   +7 more
wiley   +1 more source

Understanding atrioventricular septal defect: Anatomoechocardiographic correlation-12

, 2011
Lar septum and the interchordal spaces (asterisks) that create the ventricular septal defect. (B) The two-dimensional echocardiographic 4-chamber image shows the same features as in the anatomic specimen.
Luis Muñoz-Castellanos (39502), Magdalena Kuri-Nivón (39504), Candace Keirns (39505), Nilda Espinola-Zavaleta (39503)   +3 more
core   +1 more source

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin–Siris Syndrome and Sialuria From India

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Coffin–Siris syndrome (CSS) (OMIM:614608) is a rare genetic disorder characterized by global developmental delay (GDD), speech impediment, coarse facial features, and hypoplastic or absent fifth fingernails/toenails. Genetic variants in the SMARCB1 gene are associated with CSS, benign tumors (schwannomas), and rhabdoid tumor predisposition ...
Aparna Bhanushali, Archana Kawalakatt, Smita Kulkarni, Preethi Nair, Ankita Mali, Ashlesha Pradhan, Anirvan Chatterjee   +6 more
wiley   +1 more source

Rapidly Progressive Bilateral Infective Endocarditis Involving Prosthetic Material After Repaired Tetralogy of Fallot: A Case Report

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Infective endocarditis after repaired tetralogy of Fallot can rapidly progress when prosthetic material is involved. We report bilateral multivalvular endocarditis undetected by transthoracic echocardiography but identified by transesophageal echocardiography.
Hiroki Ikeuchi, Masao Hirano, Masashi Kabasawa   +2 more
wiley   +1 more source

Complete atrioventricular septal defect and Ebstein anomaly.

, 1996
The newborn reported here presented with congestive heart failure and cyanosis on the first day of life. Echocardiographic examination revealed complete atrioventricular septal defect and Ebstein anomaly, a rare combination that has not been previously ...
Guenthard J, Wyler F
core   +1 more source

Premature Ductus Arteriosus Constriction and Pulmonary Trunk Dilation in a Case of Non‐Immune Hydrops Fetalis With Trisomy 21

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Premature constriction of the ductus arteriosus accompanied by the dilation of the pulmonary trunk constitutes a rare congenital heart anomaly that may be underestimated and can result in fetal hydrops and ultimately death if not treated; therefore, it necessitates fetal post‐mortem evaluation in all cases of legal abortion or fetal death.
Nazari Mohadeseh, Hejrati Zinatosadat, Pajokh Mojde   +2 more
wiley   +1 more source

Complete atrioventricular canal

Orphanet Journal of Rare Diseases, 2006
Complete atrioventricular canal (CAVC), also referred to as complete atrioventricular septal defect, is characterised by an ostium primum atrial septal defect, a common atrioventricular valve and a variable deficiency of the ventricular septum inflow ...
Limongelli Giuseppe, Calabrò Raffaele
doaj   +1 more source

Congenital heart disease in pregnancy and severe maternal morbidity: A distributed data network study

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, Benjamin Martin, Xiao Xu, Anna Booman, Alyssa Howren, Kimberlee McKay, Sadaf Kazi, Sean O'Reilly, Katie S. Kolla, Khyzer Aziz, Katherine Bianco, Stephanie A. Leonard   +11 more
wiley   +1 more source

The current surgical perspective to repair of atrioventricular septal defect with common atrioventricular junction

, 2010
Atrioventricular septal defect with common atrioventricular junction is a relatively common congenital cardiac malformation. It sometimes presents challenging surgical problems, especially when seen in combination with tetralogy of Fallot.
Anderson, Robert H., Sylvio C. J. Provenzano, Provenzano, Sylvio C. J., Nunn, Graham R., Karl, Tom R., Tom R. Karl, Robert H. Anderson, Graham R. Nunn   +7 more
core   +1 more source