Cargando…

Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence

BACKGROUND: Follow‐up cytogenetic analysis has been recommended for cases with positive noninvasive prenatal screening (NIPS) results. This study of five cases with numerical and structural sex chromosomal abnormalities (SCA) and a review of large case series of NIPS provided guidance to improve pre...

Descripción completa

Detalles Bibliográficos
Autores principales:	Xie, Xiaolei, Tan, Weihe, Li, Fuguang, Carrano, Eric, Ramirez, Paola, DiAdamo, Autumn, Grommisch, Brittany, Amato, Katherine, Chai, Hongyan, Wen, Jiadi, Li, Peining
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2020
Materias:	Review Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336728/ https://www.ncbi.nlm.nih.gov/pubmed/32383339 http://dx.doi.org/10.1002/mgg3.1297

Ejemplares similares

Integrated FISH, Karyotyping and aCGH Analyses for Effective Prenatal Diagnosis of Common Aneuploidies and Other Cytogenomic Abnormalities
por: Chai, Hongyan, et al.
Publicado: (2019)

Genotype–Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature
por: Xie, Xiaolei, et al.
Publicado: (2022)

Analytical validation and chromosomal distribution of regions of homozygosity by oligonucleotide array comparative genomic hybridization from normal prenatal and postnatal case series
por: Wen, Jiadi, et al.
Publicado: (2019)

Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin
por: Zerjav, Marie, et al.
Publicado: (2020)

Inverted duplication, triplication and quintuplication through sequential breakage‐fusion‐bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion
por: Chai, Hongyan, et al.
Publicado: (2019)

Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma
por: Chai, Hongyan, et al.
Publicado: (2022)

A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings
por: Chai, Hongyan, et al.
Publicado: (2019)

Detection of cytogenomic abnormalities by OncoScan microarray assay for products of conception from formalin-fixed paraffin-embedded and fresh fetal tissues
por: Wen, Jiadi, et al.
Publicado: (2021)

Changes in and Efficacies of Indications for Invasive Prenatal Diagnosis of Cytogenomic Abnormalities: 13 Years of Experience in a Single Center
por: Meng, Jinlai, et al.
Publicado: (2015)

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia
por: Bajaj, Renu, et al.
Publicado: (2011)

The Effect of Freezing on Non-invasive Prenatal Testing
por: Xie, Xiaolei, et al.
Publicado: (2019)

Combined Use of Cytogenetic and Molecular Methods in Prenatal Diagnostics of Chromosomal Abnormalities
por: Stomornjak-Vukadin, Meliha, et al.
Publicado: (2015)

Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis
por: Yu, Mullin Ho Chung, et al.
Publicado: (2021)

Noninvasive prenatal testing detects microdeletion abnormalities of fetal chromosome 15
por: Yin, Lianli, et al.
Publicado: (2019)

Positive predictive value of noninvasive prenatal testing for sex chromosome abnormalities
por: Guo, Nan, et al.
Publicado: (2022)

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

Analysis of the clinical features of pericentric inversion of chromosome 9
por: Xie, Xiaolei, et al.
Publicado: (2020)

Jumping Translocations of 1q in Myelodysplastic Syndrome and Acute Myeloid Leukemia: Report of Three Cases and Review of Literature
por: Couture, T., et al.
Publicado: (2018)

Age and cytogenetic abnormalities()
por: Souza, Cármino Antonio de
Publicado: (2018)

Cytogenetic microarray in prenatal and postnatal diagnosis
por: Phadke, Shubha
Publicado: (2014)

Study on the Clinical Value of Noninvasive Prenatal Testing in Screening the Chromosomal Abnormalities of the Fetus in the Elderly Pregnant Women
por: Gu, Zhiping, et al.
Publicado: (2022)

Prenatal genetic testing in 19 fetuses with corpus callosum abnormality
por: She, Qin, et al.
Publicado: (2021)

Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis
por: Yang, Yang, et al.
Publicado: (2023)

Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern China
por: Yang, Jiexia, et al.
Publicado: (2021)

Cytogenetic abnormalities in Langerhans cell histiocytosis.
por: Betts, D. R., et al.
Publicado: (1998)

Rare Cytogenetic Abnormalities in Myelodysplastic Syndromes
por: Bacher, Ulrike, et al.
Publicado: (2015)

Cytogenetic Abnormalities in Myelodysplastic Syndromes: An Overview
por: Zahid, Mohammad Faizan, et al.
Publicado: (2017)

Prognostic Impact of Cytogenetic Abnormalities in Multiple Myeloma: A Retrospective Analysis of 229 Patients
por: Jian, Yuan, et al.
Publicado: (2016)

Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalities
por: Xu, Zhiyong, et al.
Publicado: (2014)

Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses
por: Peng, Gang, et al.
Publicado: (2023)

Cytogenetical studies in five Atlantic Anguilliformes fishes
por: Vasconcelos, Antonio Jales Moraes, et al.
Publicado: (2009)

Extended homozygosity is not usually due to cytogenetic abnormality
por: Curtis, David
Publicado: (2007)

Cytogenetic and molecular abnormalities in chronic myelomonocytic leukemia
por: Patnaik, M M, et al.
Publicado: (2016)

Cytogenetic Abnormalities Found in Patients with Reproductive Problems
por: Mackic-Djurovic, Mirela, et al.
Publicado: (2017)

Molecular diagnosis of cytogenetic abnormalities in patients with schizophrenia
por: Bar Shai, M., et al.
Publicado: (2022)

Prenatal diagnosis and molecular cytogenetic analysis of a de novo isodicentric chromosome 18
por: Zhang, Yanliang, et al.
Publicado: (2010)

Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis
por: Xue, Huili, et al.
Publicado: (2020)

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
por: Jiang, Fuman, et al.
Publicado: (2012)

Application of ultrasound combined with noninvasive prenatal testing in prenatal testing
por: Liu, Ci, et al.
Publicado: (2022)

Noninvasive Prenatal Measurement of the Fetal Genome
por: Fan, H. Christina, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_tid4dcrqdki9atrf5b2du8el92