Results 51 to 60 of about 600,328 (248)

Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study

Molecular Cytogenetics
Background The 15q11.2 BP1-BP2 microdeletion syndrome is associated with developmental delays, language impairments, neurobehavioral disorders, and psychiatric complications.
Jianlong Zhuang, Na Zhang, Wanyu Fu, Yuying Jiang, Yu’e Chen, Chunnuan Chen   +5 more
doaj   +1 more source

Intra-uterine fetal demise caused by amniotic band syndrome after standard amniocentesis [PDF]

, 2000
The amniotic band syndrome represents a prime example of exogenous disruption of an otherwise normal feta I development. It may be a sequel of invasive diagnostic procedures such as amniocentesis or fetal blood sampling. A 38-year-old gravida II, para II
Bauerfeind, I., Hasbargen, U., Hepp, Hermann, Strauss, Alexander, Paek, Bettina   +4 more
core   +1 more source

Prenatal diagnosis and molecular cytogenetic analysis of pure chromosome 10p15.3 microdeletion using chromosomal microarray analysis

BMC Medical Genomics
Background The literature contains exceedingly limited reports on chromosome 10p15.3 microdeletions. In the present study, two cases of fetuses with pure terminal 10p15.3 microdeletion syndrome in a Chinese population were examined, with the objective of
Na Zhang, Nan Huang, Yu’e Chen, Xinying Chen, Jianlong Zhuang   +4 more
doaj   +1 more source

Optimal timing for induction of labor in normotensive women: A retrospective cohort study

International Journal of Gynecology &Obstetrics, Volume 169, Issue 1, Page 365-371, April 2025.
Abstract Objective Labor induction is offered to reduce the risk of stillbirth at late term (41+0 to 41+6) but earlier induction in normotensive singleton pregnancies is supported by weak evidence. The aim of the present study was to investigate the optimal timing for induction in normotensive women.
Jóhanna Gunnarsdóttir, Emma Marie Swift, Alexander Smárason, Kristjana Einarsdóttir   +3 more
wiley   +1 more source

Timing of first prenatal ultrasound and associated factors among women who gave birth at health institutions in Ambo Town, central Ethiopia.

PLoS ONE
BackgroundThe Ethiopian Ministry of Health recommends "one prenatal ultrasound scan before 24 weeks of gestation for every pregnant woman." Despite clear suggestions for timely prenatal ultrasound utilization, little is known about the extent to which it
Samson Mesfin, Gizachew Abdissa Bulto, Motuma Gutu, Natnael Dechasa Gemeda   +3 more
doaj   +1 more source

Evaluation of a novel fetal echocardiography training programme in two tertiary care obstetric Centres

International Journal of Gynecology &Obstetrics, EarlyView.
Abstract Objectives Improving and maintaining high detection rates for major congenital heart disease (CHD) is a priority for successful prenatal anatomy screening programmes. The primary objective of this study was to evaluate the utility of on‐site multidimensional targeted training in fetal cardiac screening. Methods A prospective study evaluating a
Fiona Cody, Orla Franklin, Caoimhe Lynch, Zara Molphy, Patrick Dicker, Fergal Malone, Fionnuala M. Breathnach   +6 more
wiley   +1 more source

EVALUATION OF THE INCIDENCE AND OUTCOME OF FETAL HYDRONEPHROSIS PRENATALLY DIAGNOSED BY ULTRASOUND [PDF]

The outcome and proper management of fetal hydronephrosis have not been completely defined. The purpose of this study was to determine incidence and outcome of infants with a history of prenatal hydronephrosis diagnosed by ultrasound.
رفاهی, سهیلا, پورعیسی, مسعود, نظری, حسین   +2 more
core  

Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases

, 2021
Bulleted Statements: What's already known about this topic? The incidence of discordant fetal sex was estimated to be 1 in 1500-2000. Comprehensive evaluation is required to investigate the underlying cause. What does this study add?
Ma, TWL, Li, EYY, Chan, KYK, Man, E, Kong, MCW, Yu, FNY, Chung, BHY, Kan, ASY   +7 more
core   +1 more source

Prenatal diagnose of a fetus with Harlequin ichthyosis in a Chinese family

Taiwanese Journal of Obstetrics & Gynecology, 2018
Objective: Harlequin ichthyosis (HI) was the most severe form of ichthyoses, which leaded to neonatal death in 50% of cases. It was the result of mutations in ABCA12 gene.
Wei Jian, Qi-Ting Du, Zhen-Fei Lai, Yu-Fan Li, Shi-Quan Li, Zhong-Tang Xiong, Dun-Jin Chen, Min Chen, Jing-Si Chen   +8 more
doaj   +1 more source

Dyssegmental dysplasia, Silverman-Handmaker type: prenatal ultrasound findings and molecular analysis.

, 2013
OBJECTIVES: The objective of this study is to describe the prenatal sonographic features and the results of DNA analysis on three fetuses with dyssegmental dysplasia, Silverman-Handmaker type (DD-SH). METHODS: A retrospective review of three fetuses with
Chitayat, D., Glanc, P., Nezarati, M.M., Velsher, L., Keating, S., Silver, R.J., Laureane, M.C., Unger, S., Ladhani, N.N., Sirkin, W., Toi, A.   +10 more
core   +1 more source