Cargando…

Follow-up in Patients With Non-invasive Prenatal Screening Failures: A Reflection on the Choice of Further Prenatal Diagnosis

BACKGROUND: Our aim was to provide a theoretical basis for clinicians to conduct genetic counseling and choose further prenatal diagnosis methods for pregnant women who failed non-invasive prenatal screening (NIPS). METHODS: A retrospective analysis was performed on pregnant women who had failed NIP...

Descripción completa

Detalles Bibliográficos
Autores principales:	Liu, Sha, Liu, Hongqian, Liu, Jianlong, Bai, Ting, Jing, Xiaosha, Xia, Tianyu, Deng, Cechuan, Liu, Yunyun, Cheng, Jing, Wei, Xiang, Xing, Lingling, Luo, Yuan, Zhou, Quanfang, Zhu, Qian
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172122/ https://www.ncbi.nlm.nih.gov/pubmed/34093659 http://dx.doi.org/10.3389/fgene.2021.666648

Ejemplares similares

Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China
por: Jing, Xiaosha, et al.
Publicado: (2022)

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

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

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

Clinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital
por: Deng, Cechuan, et al.
Publicado: (2019)

Factors Affecting the Fetal Fraction in Noninvasive Prenatal Screening: A Review
por: Deng, Cechuan, et al.
Publicado: (2022)

Qualifying choice: ethical reflection on the scope of prenatal screening
por: Stapleton, Greg
Publicado: (2016)

Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis
por: Liu, Xijing, et al.
Publicado: (2022)

Clinical experience of noninvasive prenatal testing for rare chromosome abnormalities in singleton pregnancies
por: Hu, Ting, et al.
Publicado: (2022)

Clinical Utility of the Prenatal BACs-on-Beads™ Assay in Invasive Prenatal Diagnosis
por: Jiang, Yu, et al.
Publicado: (2022)

The Optimal Cutoff Value of Z-scores Enhances the Judgment Accuracy of Noninvasive Prenatal Screening
por: Zhou, Lingna, et al.
Publicado: (2021)

Placental DNA Methylation Abnormalities in Prenatal Conotruncal Heart Defects
por: Liu, Jingjing, et al.
Publicado: (2022)

A spectrum of clinical severity of recessive titinopathies in prenatal
por: Qi, Yiming, et al.
Publicado: (2023)

Molecular Diagnosis and Prenatal Phenotype Analysis of Eight Fetuses With Ciliopathies
por: Liu, Yuefang, et al.
Publicado: (2021)

Case report: identification of one frameshift variant and two in cis non-canonical splice variants of NEB gene in prenatal arthrogryposis
por: Liu, Yuefang, et al.
Publicado: (2023)

Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort
por: Yi, Tong, et al.
Publicado: (2022)

Prenatal diagnosis and outcomes in 320 fetuses with nasal bone anomalies
por: Li, Hui, et al.
Publicado: (2023)

A retrospective single-center analysis of prenatal diagnosis and follow-up of 626 chinese patients with positive non-invasive prenatal screening results
por: Bu, Xiufen, et al.
Publicado: (2022)

Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing
por: Yu, Jialing, et al.
Publicado: (2022)

Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies
por: Ji, Xiuqing, et al.
Publicado: (2018)

Ethical, Legal and Social Issues (ELSI) Associated with Non-Invasive Prenatal Testing: Reflections on the Evolution of Prenatal Diagnosis and Procreative Choices
por: Zaami, Simona, et al.
Publicado: (2021)

Next-generation sequencing: a follow-up of 36,913 singleton pregnancies with noninvasive prenatal testing in central China
por: Lu, Wan, et al.
Publicado: (2020)

Effective Identification of Maternal Malignancies in Pregnancies Undergoing Noninvasive Prenatal Testing
por: Li, Jia, et al.
Publicado: (2022)

Mutation detection and prenatal diagnosis of XLHED pedigree
por: Lin, Yao, et al.
Publicado: (2017)

Paternal Tobacco Smoke Correlated to Offspring Asthma and Prenatal Epigenetic Programming
por: Wu, Chih-Chiang, et al.
Publicado: (2019)

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies
por: Xiang, Jingjing, et al.
Publicado: (2020)

Comprehensive Evaluation of Non-invasive Prenatal Screening to Detect Fetal Copy Number Variations
por: Wang, Jing, et al.
Publicado: (2021)

Prenatal Exposure to a Climate-Related Disaster Results in Changes of the Placental Transcriptome and Infant Temperament
por: Buthmann, Jessica, et al.
Publicado: (2022)

46,XX Testicular Disorders of Sex Development With DMD Gene Mutation: First Case Report Identified Prenatally by Integrated Analyses in China
por: Deng, Jianlian, et al.
Publicado: (2020)

The Added Value of Whole-Exome Sequencing for Anomalous Fetuses With Detailed Prenatal Ultrasound and Postnatal Phenotype
por: He, Miao, et al.
Publicado: (2021)

A Randomized Controlled Trial on the Influence of Prenatal Counseling on the Attitudes and Preferences Toward Invasive Prenatal Testing Among Women in Their First Trimester of Pregnancy (INVASIVE)
por: Paz y Miño, Fernanda, et al.
Publicado: (2020)

Maternal Xp22.31 copy-number variations detected in non-invasive prenatal screening effectively guide the prenatal diagnosis of X-linked ichthyosis
por: Tang, Xinxin, et al.
Publicado: (2022)

Schaaf-Yang Syndrome: A Real Challenge for Prenatal Diagnosis
por: Nunes, Sara, et al.
Publicado: (2021)

Performance of noninvasive prenatal testing for twin pregnancies in South China
por: Wang, Dongmei, et al.
Publicado: (2023)

Optical genome mapping in an atypical Pelizaeus-Merzbacher prenatal challenge
por: Rogac, Mihael, et al.
Publicado: (2023)

Patient attitudes and preferences about expanded noninvasive prenatal testing
por: Dubois, Marie-Line, et al.
Publicado: (2023)

Editorial: Unravelling the basis of non-invasive prenatal screening results
por: De Falco, Luigia, et al.
Publicado: (2023)

Case Report: Candidate Genes Associated With Prenatal Ultrasound Anomalies in a Fetus With Prenatally Detected 1q23.3q31.2 Deletion
por: Song, Jiahao, et al.
Publicado: (2021)

Non-Invasive Prenatal Diagnosis of Monogenic Disorders Through Bayesian- and Haplotype-Based Prediction of Fetal Genotype
por: Li, Jia, et al.
Publicado: (2022)

Case report: Prenatal diagnosis of rare chromosome mosaicism: discordant results between chorionic villi and amniotic fluid samples
por: Li, Lingping, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_nho0oa3e17i16arakkeivmiaek