Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China

Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China

Background: This study aims to evaluate prenatal diagnosis methods following positive noninvasive prenatal screening (NIPS) results.Methods: According to the positive noninvasive prenatal screening results, 926 pregnant women were divided into three groups: main target disease group (high risk for t...

Full description

Bibliographic Details
Main Authors:	Xiaosha Jing, Hongqian Liu, Qian Zhu, Sha Liu, Jianlong Liu, Ting Bai, Cechuan Deng, Tianyu Xia, Yunyun Liu, Jing Cheng, Xiang Wei, Lingling Xing, Yuan Luo, Quanfang Zhou, Lin Chen, Lingping Li, Jiamin Wang
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2022-01-01
Series:	Frontiers in Genetics
Subjects:	aneuploidy noninvasive prenatal screening sex chromosome mosaicism other chromosomal abnormalities positive NIPS results prenatal diagnostic techniques
Online Access:	https://www.frontiersin.org/articles/10.3389/fgene.2021.811414/full

Similar Items

Follow-up in Patients With Non-invasive Prenatal Screening Failures: A Reflection on the Choice of Further Prenatal Diagnosis
by: Sha Liu, et al.
Published: (2021-05-01)

Noninvasive Prenatal Screening Based on Second-Trimester Ultrasonographic Soft Markers in Low-Risk Pregnant Women
by: Yunyun Liu, et al.
Published: (2021-12-01)

Maternal and fetal factors influencing fetal fraction: A retrospective analysis of 153,306 pregnant women undergoing noninvasive prenatal screening
by: Cechuan Deng, et al.
Published: (2023-04-01)

Maternal, neonatal, pregnancy outcome characteristics of pregnant women with high plasma cell-free DNA concentration in non-invasive prenatal screening: a retrospective analysis
by: Lingling Xing, et al.
Published: (2023-08-01)

Identification of copy number variations among fetuses with isolated ultrasound soft markers in pregnant women not of advanced maternal age
by: Yunyun Liu, et al.
Published: (2024-02-01)

Clinical experience of noninvasive prenatal testing for rare chromosome abnormalities in singleton pregnancies
by: Ting Hu, et al.
Published: (2022-09-01)

Combined use of bacterial artificial chromosomes-on-beads with karyotype detection improves prenatal diagnosis
by: Zhengyou Miao, et al.
Published: (2019-02-01)

Factors Affecting the Fetal Fraction in Noninvasive Prenatal Screening: A Review
by: Cechuan Deng, et al.
Published: (2022-01-01)

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies
by: Jingjing Xiang, et al.
Published: (2020-11-01)

Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis
by: Xijing Liu, et al.
Published: (2022-07-01)

Case report: Prenatal diagnosis of rare chromosome mosaicism: discordant results between chorionic villi and amniotic fluid samples
by: Lingping Li, et al.
Published: (2023-06-01)

Prenatal Diagnosis and Pregnancy Outcome Analysis of High-risk Fetuses Suggested by Noninvasive Prenatal Screening
by: Yan LUO, Bingyi ZHAO, Yanmei SUN, Haishen TIAN, Yali LI, Yanshang ZHANG, Jian GAO, Zhiqiang CUI
Published: (2022-07-01)

Perinatal outcomes of prenatal cases testing positive for trisomy 9 by noninvasive prenatal testing
by: Hui Li, et al.
Published: (2022-11-01)

Application of chromosome microarray analysis in prenatal diagnosis
by: Mingjing Xia, et al.
Published: (2020-11-01)

Prenatal diagnosis of a novel 7q31.31q31.33 microduplication with a favorable outcome
by: Huili Luo, et al.
Published: (2022-03-01)

Amniotic fluid karyotype analysis and prenatal diagnosis strategy of 3117 pregnant women with amniocentesis indication
by: Yi Liu, et al.
Published: (2023-05-01)

Submicroscopic aberrations of chromosome 16 in prenatal diagnosis
by: Xiaoqing Wu, et al.
Published: (2019-08-01)

Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature
by: Xiao-Nan Hu, et al.
Published: (2021-05-01)

Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese family
by: Wenjuan Tang, et al.
Published: (2022-07-01)

Positive predictive value estimates for noninvasive prenatal testing from data of a prenatal diagnosis laboratory and literature review
by: Siping Liu, et al.
Published: (2022-07-01)

Prenatal Sonographic Features of Rare Chromosome 13 Aberrations
by: Moczulska H, et al.
Published: (2022-10-01)

Frequency and clinical manifestation of prenatal cytogenetic diagnosis of chromosomal polymorphisms in Northeast China
by: Li-Li Luo, et al.
Published: (2020-11-01)

Prenatal diagnosis and genetic counseling of an inherited unbalanced chromosome abnormalities in a Chinese family
by: Ying Zhang, et al.
Published: (2022-08-01)

Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis
by: Yang Yang, et al.
Published: (2023-09-01)

Prenatal diagnosis and genetic counseling of an inherited Xq24q25 deletion associated with normal phenotype
by: Yaqing Zhou, et al.
Published: (2022-11-01)

Trends in Non-invasive Prenatal Screening and Invasive Testing in Denmark (2000–2019) and Israel (2011–2019)
by: Lena Sagi-Dain, et al.
Published: (2021-11-01)

Prenatal diagnosis: A connotation on genetic counseling being indispensable
by: Anuradha Ramesh, et al.
Published: (2020-01-01)

Clinical value of genetic analysis in prenatal diagnosis of short femur
by: Jialiu Liu, et al.
Published: (2019-11-01)

Cell-free fetal DNA testing and its correlation with prenatal indications
by: Jing-wei Wang, et al.
Published: (2021-08-01)

Prenatal Diagnosis and Fetal Outcomes of Cystic Hygroma: Experience of a Tertiary Hospital
by: Betul Yakistiran, et al.
Published: (2019-04-01)

Segmental duplication as potential biomarkers for non-invasive prenatal testing of aneuploidies
by: Xinwen Chen, et al.
Published: (2021-08-01)

Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report
by: Reza Mohammadi, et al.
Published: (2021-05-01)

Maternal mosaicism of sex chromosome causes discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing
by: Leilei Wang, et al.
Published: (2015-10-01)

Prenatal Sonographic Features of Ring Chromosome 15: A Case Report and Literature Review
by: Kuntharee Traisrisilp, et al.
Published: (2022-04-01)

THE INCIDENCE AND TYPE OF CHROMOSOMAL TRANSLOCATIONS FROM PRENATAL DIAGNOSIS OF 3800 PATIENTS IN THE REPUBLIC OF MACEDONIA
by: Vasilevska M., et al.
Published: (2013-12-01)

Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype
by: Jieping Song, et al.
Published: (2022-06-01)

Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China
by: Ganye Zhao, et al.
Published: (2022-01-01)

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11
by: Chih-Ping Chen, et al.
Published: (2017-06-01)

Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies
by: Hua Hu, et al.
Published: (2019-03-01)

Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities
by: Shanning Wan, et al.
Published: (2019-05-01)