Results 71 to 80 of about 3,319 (201)

NONO‐Related Syndromic X‐Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal Cohort

Prenatal Diagnosis, Volume 46, Issue 5-6, Page 914-923, May 2026.
ABSTRACT Objective To characterize the prenatal sonographic features across different trimesters and genomic spectrum of NONO‐related X‐linked intellectual developmental disorder. Method We analyzed two fetuses presenting with corpus callosum agenesis and rare cardiac anomalies using genome sequencing and exome sequencing.
Yilin Zhao, Gang Zou, Mengmeng Shi, Kwok Ming Law, So Ling Lau, Meng Meng, Yuen Ha Ting, Chiu Yee Liona Poon, Zirui Dong, Matthew Hoi Kin Chau, Tak Yeung Leung, Kwong Wai Choy, Xinwen Zhang, Ye Cao   +13 more
wiley   +1 more source

The EUROmediCAT Network and Databases: A Resource for Pharmacovigilance in Pregnancy

Pharmacoepidemiology and Drug Safety, Volume 35, Issue 5, May 2026.
ABSTRACT Background The evidence gap relating to the risk of congenital anomalies (CA) associated with first trimester medication exposure in pregnancy is well recognized. Aims We describe the EUROmediCAT network and databases, and the methodological approach to pregnancy pharmacovigilance.
Helen Dolk, Christine Damase‐Michel, Joan Morris, Amanda Neville, Ester Garne, Sue Jordan, Anke Rissmann, Alessio Coi, Deirdre Folan, Dieuwke Broekstra, Jennifer M. Broughan, Lea Bruneau, Clara Cavero‐Carbonell, Elly den Hond, Miriam Gatt, Mika Gissler, Babak Khoshnood, Anna Latos Bielenska, Hedvig Nordeng, Ljubica Odak, Mary O'Mahony, Isabelle Perthus, J. Luke Richardson, Florence Rouget, Joanna Sichitiu, David Tucker, Natalya Zymak‐Zakutnya, Maria Loane   +27 more
wiley   +1 more source

Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network

Paediatric and Perinatal Epidemiology, Volume 40, Issue 3, Page 414-425, March 2026.
ABSTRACT Background Surveillance of congenital anomaly prevalence over time can identify new teratogens. Anomalies with a genetic cause are excluded from the monitoring. Objectives We examined temporal changes in the proportion of genetic diagnoses among cases with a congenital anomaly.
Jorieke E. H. Bergman, Annie Perraud, Ester Garne, Ingeborg Barisic, David Tucker, Elisa Ballardini, Lea Bruneau, Clara Cavero‐Carbonell, Ianis Cousin, Miriam Gatt, Katya Kovacheva, Anna Latos‐Bielenska, Mary O'Mahony, Isabelle Monier, Isabelle Perthus, Riccardo Pertile, Anke Rissmann, Florence Rouget, Michelle Santoro, Joanna Sichitiu, Christine Verellen‐Dumoulin, Wladimir Wertelecki, Diana Wellesley, Joan K. Morris   +23 more
wiley   +1 more source

Ebstein anomaly of the tricuspid valve in an adult cohort

, 1999
grantor: University of Toronto'Objective.' We examined the spectrum of adults with Ebstein anomaly of the tricuspid valve. 'Methods.' Clinical data, EKG, chest x-rays, echocardiograms and surgical details were reviewed in patients with Ebstein ...
Warsi, Mohammed Ali
core   +1 more source

Supraventricular Tachycardias Using Multiple Accessory Pathways

Journal of Arrhythmia, Volume 42, Issue 1, February 2026.
Three atrioventricular reciprocating tachycardias (AVRTs) using 3 accessory pathways (APs) occurred with the His bundle eliminated by the previous ablation. Two AVRTs using 2 right APs rotated reversely, and the other AVRT was one with a retrograde conduction through the left AP and anterograde conduction through the 2 right APs.
Takumi Yamada
wiley   +1 more source

Management and long-term outcome of neonatal Ebstein anomaly

, 2009
ObjectiveThe objective of this study was to review the long-term results of symptomatic patients with Ebstein anomaly in the neonatal period.MethodsThe medical records of 40 neonates with a diagnosis of Ebstein anomaly who were admitted to our ...
Richard G. Ohye, Carlen A. Gomez-Fifer, Bove, Edward L., Jennifer C. Hirsch, Ohye, Richard G., Hirsch, Jennifer C., Takeshi Shinkawa, Edward L. Bove, Anastasios C. Polimenakos, Devaney, Eric J., Charpie, John R., Shinkawa, Takeshi, Polimenakos, Anastasios C., Eric J. Devaney, John R. Charpie, Gomez-Fifer, Carlen A.   +15 more
core   +1 more source

Maternal Myo‐Inositol Intake and Congenital Heart Defects in Offspring: A Population‐Based Case–Control Study

BJOG: An International Journal of Obstetrics &Gynaecology, Volume 133, Issue 3, Page 442-453, February 2026.
ABSTRACT Objective To investigate associations between maternal periconceptional (three months prior through the third pregnancy month) myo‐inositol intake and the odds of selected congenital heart defects in offspring. Design A population‐based case–control study using the National Birth Defects Prevention Study (NBDPS) database. Setting United States.
Ruiqi Cen, L. Joseph Su, Jun Ying, Mohammed S. Orloff, Elijah H. Bolin, Xiangyang Lou, Lynn M. Almli, Lorenzo D. Botto, Marilyn L. Browne, Richard H. Finnell, Mary M. Jenkins, Eirini Nestoridi, Andrew F. Olshan, Paul A. Romitti, Gary M. Shaw, Wendy N. Nembhard, the National Birth Defects Prevention Study   +16 more
wiley   +1 more source

Complex Ebstein\'s Anomaly In A 80year Old Nigerian Woman

, 2008
There is a gradually growing interest in the subject of congenital heart diseases as many children born with them are now growing into adulthood. The reasons are twofold: increasing awareness among clinicians as well as major advances in the diagnosis ...
Ukoh, V A, Adesanya, A A
core   +1 more source

Grit in the Workplace Experienced by Taiwanese Adults With Congenital Heart Disease: A Phenomenological Study

Journal of Clinical Nursing, Volume 35, Issue 2, Page 866-878, February 2026.
ABSTRACT Aim To explore how adults with congenital heart disease (ACHD) experience and express grit in the workplace. Design Qualitative study using Husserl's descriptive phenomenology. Methods Between March 2022 and June 2023, semi‐structured interviews were administered to 18 ACHD recruited from two medical centre outpatient departments.
Yu‐Shiu Liu, Chun‐Wei Lu, Hung‐Tao Chung, Jou‐Kou Wang, Ying‐Mei Shu, Chi‐Wen Chen   +5 more
wiley   +1 more source

Electrophysiologic Considerations in Adult Patients with Ebstein’s Anomaly

Ebstein’s anomaly (EA) is a rare cyanotic form of congenital heart disease (CHD) characterized by apical displacement of the tricuspid valve, with resultant hemodynamic and electrical manifestations.
Komandoor Srivathsan, Olubadewa A. Fatunde, Ingrid Hsiung, Malini Madhavan, David S. Majdalany   +4 more
core   +1 more source