Results 111 to 120 of about 1,224,037 (184)

Ivemark syndrome in an adult with complete atrioventricular septal defect and a single ventricle with L-transposition of the great arteries: a case report

Journal of Medical Case Reports
Background Ivemark syndrome is a rare heterotaxy disorder characterized by right atrial isomerism, complex congenital heart defects, and thoraco-abdominal anomalies. Because of such defects, survival beyond infancy is rare.
Hind Hibatouallah, Samah El-Mhadi, Selma Siagh, Zakia Touati, Mohamed Cherti   +4 more
doaj   +1 more source

Tracing Colonial Continuities: Internal Colonialism and Energy Transition in Sardinia

Antipode, Volume 58, Issue 6, November 2026.
ABSTRACT Internal colonialism provides historical and structural conditions making current forms of energy extractivism possible. Processes through which earlier internal colonisation operated—territorial dispossession, racialised hierarchies, forced modernisation and the construction of internal ‘Others’—are reactivated today under the global ...
Martina Loi, Alice Salimbeni
wiley   +1 more source

Assessing quality standards of biomarker measurement in first‐trimester combined screening for preeclampsia in the Chinese population: A multicenter study

Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 11, Page 2285-2294, November 2026.
In 22 066 first‐trimester pregnancies from six Chinese hospitals, biomarker measurements required recalibration to align with the established risk model. Continuous quality assurance is essential to ensure accurate preeclampsia risk assessment when implementing combined screening in new populations.
Jiao Liu, Xiaotian Li, Huixia Yang, Qiongjie Zhou, Hao Ying, Rong Zhou, Yanping Zhang, Wang Xueyin, Han Xie, Xinzhi Tu, Lin Kong, Jie Qin, Chi Chiu Wang, Xiaohong Lu, Long Nguyen‐Hoang, Daljit S. Sahota, Liona C. Poon   +16 more
wiley   +1 more source

Unravelling the complexity of heterotaxy syndrome. [PDF]

BMJ Case Rep, 2023
Bilamge A, Vallabhaneni P, Didel S, Rajagopal R.   +3 more
europepmc   +1 more source

Prediction of coarctation of the aorta in fetuses with transposition of great arteries: Inverted ventricular discrepancy as a predictor of arch repair in TGA

Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 11, Page 2359-2366, November 2026.
Fetal MV/TV ratio offers a simple and reproducible marker of AAO in TGA with a cutoff of ≥ 1.0 accurately predicting the need for arch repair. This simple echocardiographic marker improves prenatal risk stratification and surgical planning, facilitating prenatal counseling. Abstract Introduction Transposition of great arteries (TGA) with coarctation of
Cosimo Marco Campanale, Patrizio Moras, Serena Ventrella, Marco Masci, Luciano Pasquini, Alessandra Toscano   +5 more
wiley   +1 more source

A Rare Syndromic Coexistence: Bilateral Duplicated Collecting Systems with Bilateral Ureterovesical Junction Obstruction in a Child with Heterotaxy Syndrome and Polysplenia: A Case Report

Dr. Sulaiman Al Habib Medical Journal
The simultaneous occurrence of bilateral duplicated collecting systems and heterotaxy syndrome is extremely rare, with no previously reported cases from our setting to our knowledge.
Zubeir Zubeir, Zuhura Nkrumbih, Gerald Mpemba   +2 more
doaj   +1 more source

Genetics in Heterotaxy: A Case Series and Literature Review on DNAH9, PKD1L1, MMP21, and GDF1

Clinical Genetics, Volume 110, Issue 5, Page 574-583, November 2026.
Integrating trio‐based genomic sequencing with detailed clinical evaluation across seven French–Vietnamese heterotaxy cases alongside a review of 108 published patients reveals strong genotype–phenotype correlations. Variants in DNAH9, PKD1L1, MMP21, and GDF1 define a broad spectrum from isolated situs inversus to complex conotruncal heart defects and ...
Thi Bich Tuyen Ho, Alicia Coudert, Thi Thuy Hang Do, Thi Thanh Thuy Le, Marjolaine Gauthier, Charlotte Dubucs, Jeremie Mortreux, Pauline Monin, Nicolas Chatron, Françoise Devillard, Charles Coutton, Véronique Satre, Radu Harbuz, William Dufour, Louis Januel, Tristan Celse, Clara Paris, Auragen Consortium, Le Tuyet Mai Tran, Huu Tung Trinh, Pierre‐Simon Jouk, Ba Luu Truong, Thi Kim Nhi Nguyen, Julien Thevenon   +23 more
wiley   +1 more source

Intrauterine Diagnosis of Heterotaxy Syndrome

, 2009
Background Heterotaxy syndrome, including right isomerism and left isomerism, is characterized by an abnormal symmetry of the viscera and veins and is frequently associated with complex cardiac anomalies.
CHANG, CHUNG-I;WANG, JOU-KOU;WU, MEI-HWAN;SHYU, MING-KWANG;LEE, CHIEN-NAN;HSIEH, FON-JOU, 張重義;王主科;吳美環;徐明洸;李建南;謝豐舟   +1 more
core  

Increased mortality, morbidities, and costs after heart transplantation in heterotaxy syndrome and other complex situs arrangements

, 2019
Identify pediatric heart transplant (HT) recipients with heterotaxy and other complex arrangements of cardiac situs (heterotaxy/situs anomaly) and compare mortality, morbidities, length of stay (LOS), and costs to recipients with congenital heart disease
Morell, Victor O., Dodd, Debra A., Godown, Justin, Soslow, Jonathan H., Thurm, Cary, Feingold, Brian, Duong, Son Q., Hall, Matt, Sainathan, Sandeep   +8 more
core   +1 more source

RSV Disease Among Hospitalized Children: Second vs. First Year of Life Multicenter Study

Influenza and Other Respiratory Viruses, Volume 20, Issue 11, November 2026.
ABSTRACT Background Respiratory syncytial virus (RSV) is a leading cause of pediatric hospitalization, yet data on children hospitalized with RSV in their second year of life are limited. Objective To compare clinical characteristics and management practices of children hospitalized with RSV during their second versus first year of life.
Keren Armoni Domany, Inbal Golan‐Tripto, Nitzan Burrack, Kamal Masarweh, Michal Gur, Mika Rochman, Moria Be'er, Dario Prais, Meirav Mor, Moran Weinberger Opek, Elias Nasrallah, Orli Megged, Rachel Shatzman Steuerman, Michal Stein, Zohar Steinberg, Shereen Shehadeh, Aharona Glatman‐Freedman, Diana Tasher   +17 more
wiley   +1 more source