Results 81 to 90 of about 11,570 (268)

Evaluation of Nuchal Translucency Measurement in First Trimester Pregnancy [PDF]

International Journal of Fertility and Sterility, 2011
Background A significant number of pregnancies, particularly in women with previous histories of infertility, are associated with fetal abnormalities. Methods such as the nuchal translucency (NT) measurement enable us to identify more pregnancies
Mojgan Barati, Mahvash Zargar, Sara Masihi, Sima Taherpour   +3 more
doaj  

Situs Inversus Totalis: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Situs Inversus Totalis (SIT) is a rare congenital anomaly characterized by the complete mirror‐image transposition of the thoracoabdominal viscera. Although typically it has a favorable prognosis, SIT can be associated with ciliopathy‐related disorders, most notably Primary Ciliary Dyskinesia (PCD).
Xin Du, Ning Wang, Juanjuan Sheng, Yunshan Zhang, Jinfang Gao   +4 more
wiley   +1 more source

Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases [PDF]

, 2011
Genetic testing usually helps physicians to determine possible genetic diseases in unborn babies, genetic disorders of patients and the carriers who might pass the mutant gene on to their children.
Asli Subasioglu Uzak, Munis Dundar, Murat Erdogan, Yagut Akbarova   +3 more
core   +1 more source

Clinical Utility of Increased Nuchal Translucency at 11–13 Weeks of Gestation in Twin Pregnancies Based on the Chorionicity [PDF]

, 2021
Si Won Lee, Hyun-Mi Lee, You Jung Han, Moon Young Kim, H. Boo, Jin Hoon Chung   +5 more
openalex   +1 more source

CRISPR‐Cas9‐Generated TXNDC15 c.560delA Homozygous Mouse Model Exhibits Meckel–Gruber Syndrome Phenotype

genesis, Volume 64, Issue 1, February 2026.
ABSTRACT To determine whether TXNDC15 variation causes Meckel–Gruber syndrome (MKS), we assessed the pathogenicity of the frameshift variant c.560delA. A CRISPR–Cas9 generated mouse model carrying the equivalent Txndc15 c.512delA mutation was analyzed at embryonic day 15.5.
Yang Liu, Hui Wang, Liyuan Chen, Xiaoxia Wu, Zhiyong Xu, Qingfa Huang, Hu Zhang, Xiushu Cao, Xinyuan Liang, Xingjian Zhong, Caiqun Luo   +10 more
wiley   +1 more source

Ultrasonographic Fetal Nuchal Translucency Measurements and Cytogenetic Outcomes. [PDF]

JAMA Netw Open
Bellai-Dussault K, Dougan SD, Fell DB, Little J, Meng L, Okun N, Walker MC, Armour CM, Potter BK.   +8 more
europepmc   +2 more sources

Reference charts for first‐trimester placental three‐dimensional fractional moving blood volume derived using OxNNet

Ultrasound in Obstetrics &Gynecology, Volume 67, Issue 2, Page 191-200, February 2026.
ABSTRACT Objective To establish a comprehensive reference range for first‐trimester placental three‐dimensional (3D) single‐vessel fractional moving blood volume (svFMBV) using the OxNNet toolkit, based on values observed in healthy pregnancies.
S. Mathewlynn, L. N. Starck, Y. Yin, M. Soltaninejad, M. Swinburne, K. H. Nicolaides, A. Syngelaki, A. G. Contreras, S. Bigiotti, E.‐M. Woess, S. Gerry, S. Collins   +11 more
wiley   +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

Prenatal screening for down’s syndrome: parent and healthcare practitioner experiences [PDF]

, 2014
This article reviews research on both parent and healthcare practitioner experiences of prenatal screening for Down’s syndrome. Whilst studies on Down’s syndrome screening are broad in scope and diverge in theoretical and epistemological foundations ...
Thomas, Gareth Martin
core   +1 more source

VP30.11: Relation between increased fetal nuchal translucency thickness and chromosomal defects in north of Vietnam [PDF]

, 2021
Liu Hai
openalex   +1 more source