Results 51 to 60 of about 796 (160)

Prenatal Diagnosis of Fetal Hypothyroidism After Maternal Radioactive Iodine Exposure During Pregnancy

, 2010
A 33-year-old woman with a history of surgically treated papillary thyroid carcinoma was inadvertently given radioactive iodine when she was 16 weeks pregnant.
ÖZÇELİK, Bülent, Batukan, Cem, Bulent Ozcelik, Selim Kurtoglu, BAŞBUĞ, Mustafa, ÖZGÜN, Mahmut Tuncay, Murat, Nurcan, Kurtoglu, Selim, Mahmut T. Ozgun, Cem Batukan, Nurcan Murat, Mustafa Basbug   +11 more
core   +1 more source

Nipocalimab in Early‐Onset Severe Hemolytic Disease of the Fetus and Newborn

Pediatric Discovery, Volume 4, Issue 3, September 2026.
Aditya Hemedra Bhatt, Somashekhar Marutirao Nimbalkar, Dipen Vasudev Patel, Reshma Kushal Pujara   +3 more
wiley   +1 more source

Maternal Isoimmunization‐Associated Fetal Anemia After First‐Trimester Abortion: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Isoimmunization and fetal anemia pose considerable challenges in obstetrics, especially when there is a documented history of RhD incompatibility or other antibodies that may threaten fetal well‐being. These conditions frequently result in serious complications, including hydrops fetalis, fetal anemia, and, in certain situations, fetal loss ...
Fatemeh Golshahi, Behrokh sahebdel, Fatemeh Rahimi‐Sharbaf, Mahboobeh Shirazi, Nafiseh Saedi, Khadijeh Adabi, Arash Jafarieh, Maedeh Mollaalipour Amiri, Zahra Hamidi Madani   +8 more
wiley   +1 more source

Molecular Testing in Sickle Cell Disease: From Newborn Screening to Transfusion Care

International Journal of Laboratory Hematology, Volume 48, Issue 2, Page 295-304, April 2026.
ABSTRACT Sickle cell disease (SCD) is one of the most frequent monogenic diseases worldwide and a highly heterogeneous and complex disease. SCD care carries several challenges. This includes early and accurate diagnosis as well as optimal red blood cell transfusion matching in this population carrying a high risk of alloimmunization.
Thomas Pincez, Yves D. Pastore
wiley   +1 more source

Mutation analysis of the fibroblast growth factor receptor 3 gene in fetuses with thanatophoric dysplasia, type I

Clinical and Experimental Obstetrics & Gynecology, 2020
Objective: To analyze the fibroblast growth factor receptor 3 gene (FGFR3) mutations in fetuses with thanatophoric dysplasia type I (TD1) and to provide additional data for genotype-phenotype analyses.
Q.C. Wu, W.B. Wang, L. Sun, Y.S. Xu, X.J. Xie, X.M. Ma, Z.Y. Su   +6 more
doaj   +1 more source

A deep learning algorithm for automatic 3D segmentation and classification of the sheep placenta in magnetic resonance images

Physiological Reports, Volume 14, Issue 8, April 2026.
Abstract Magnetic resonance imaging (MRI) is a powerful non‐invasive method for assessing placental morphology and physiology in vivo, offering higher resolution and functional insight than ultrasound. However, placental MRI analysis is limited by manual segmentation and time‐consuming classification workflows that are prone to inter‐operator ...
Dimitra Flouri, Giorgos Adamides, Jack R. T. Darby, Stacey L. Holman, Andreas S. Panayides, Anna L. David, Vasileios Vavourakis, Janna L. Morrison, Andrew Melbourne   +8 more
wiley   +1 more source

Mosaic Trisomy 7 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses

Taiwanese Journal of Obstetrics & Gynecology, 2010
Objective: To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy 7. Materials, Methods and Results: A 38-year-old primigravid woman underwent amniocentesis at 19 weeks of gestation because of her advanced maternal age ...
Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Yuh-Ming Hwu, Shuan-Pei Lin, Chyong-Hsin Hsu, Fuu-Jen Tsai, Tao-Yeuan Wang, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Li-Feng Chen, Wayseen Wang   +12 more
doaj   +1 more source

Prenatal diagnosis and perinatal outcomes of fetuses with congenital duodenal obstruction: A nine‐year retrospective study from China

Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 2, Page 268-279, February 2026.
A retrospective study of 98 fetuses with congenital duodenal obstruction (CDO) revealed an overall genetic abnormality rate of 20.4%, with trisomy 21 being the predominant chromosomal anomaly. Comprehensive prenatal diagnostic testing is recommended for fetuses with suspected congenital duodenal obstruction, as the genetic findings exert substantial ...
Jianqin Lu, Fang Fu, Fei Guo, Hang Zhou, Ruibin Huang, Huanyi Chen, Chunling Ma, Liyuan Liu, Xiangyi Jing, Simin Yuan, Xiang Zhou, Qiuxia Yu, Manqiu Yang, Jin Han, Dongzhi Li, Ru Li, Can Liao   +16 more
wiley   +1 more source

DETECTION OF FETOMATERNAL HEMORRHAGE ASSOCIATED WITH CORDOCENTESIS USING SERUM ALPHA-FETOPROTEIN AND THE KLEIHAUER TECHNIQUE

, 1995
Fetomaternal haemorrhage (FMH) was studied after 46 cordocenteses. alpha-Fetoprotein (AFP) concentration and Kleihauer staining of maternal blood, taken both before and after the procedure, revealed increases in AFP values of more than 40 per cent in 30 ...
VANLOON, AJ, KANHAI, HHH, VANSELM, M
core   +1 more source

Low-level mosaic trisomy 21 at amniocentesis and cordocentesis in the second trimester in a pregnancy associated with positive non-invasive prenatal testing for trisomy 21, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome

Taiwanese Journal of Obstetrics & Gynecology
Objective: We present low-level mosaic trisomy 21 at amniocentesis and cordocentesis in a pregnancy associated with a favorable fetal outcome. Case Report: A 26-year-old, primigravid woman underwent amniocentesis at 17 weeks of gestation because of ...
Chih-Ping Chen, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Meng-Shan Lee, Chien-Ling Chiu, Wayseen Wang   +6 more
doaj   +1 more source