Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You or Your Team.

Learn More →

Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study

Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective... BackgroundCurrently, chromosomal microarray analysis is considered the first-tier test in pediatric care and prenatal diagnosis. However, the diagnostic yield of chromosomal microarray analysis for prenatal diagnosis of congenital heart disease has not been evaluated based on a large cohort. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png American Journal of Obstetrics and Gynecology Wolters Kluwer Health

Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study

Download PDF
17 pages

Loading next page...
 
/lp/wolters-kluwer-health/prenatal-chromosomal-microarray-analysis-in-fetuses-with-congenital-seTKTwUTeS
Publisher
Wolters Kluwer Health
Copyright
Copyright © 2017 Elsevier Inc.
ISSN
0002-9378
DOI
10.1016/j.ajog.2017.10.225
pmid
29128521
Publisher site
See Article on Publisher Site

Abstract

BackgroundCurrently, chromosomal microarray analysis is considered the first-tier test in pediatric care and prenatal diagnosis. However, the diagnostic yield of chromosomal microarray analysis for prenatal diagnosis of congenital heart disease has not been evaluated based on a large cohort.

Journal

American Journal of Obstetrics and Gynecology – Wolters Kluwer Health

Published: Feb 1, 2018

References

  • Incidence of congenital heart disease: 1, postnatal incidence
    Hoffman, J.I.E.
  • Incidence of congenital heart disease: 2, prenatal incidence
    Hoffman, J.I.E.
  • Congenital heart disease: current knowledge about causes and inheritance
    Blue, G.M.; Kirk, E.P.; Sholler, G.F.; Harvey, R.P.; Winlaw, D.S.
  • Overview of developmental heart defects by dioxins, PCBs, and pesticides
    Kopf, P.G.; Walker, M.K.
  • Importance of gene-environment interactions in the etiology of selected birth defects
    Zhu, H.; Kartiko, S.; Finnell, R.H.
  • Burden of congenital rubella syndrome (CRS) in India: a systematic review
    Dewan, P.; Gupta, P.
  • Extracardiac lesions and chromosomal abnormalities associated with major fetal heart defects: comparison of intrauterine, postnatal and postmortem diagnoses
    Song, M.S.; Hu, A.; Dyhamenahali, U.
  • Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis
    Mademont-Soler, I.; Morales, C.; Soler, A.
  • Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization
    Shearer, B.M.; Thorland, E.C.; Carlson, A.W.; Jalal, S.M.; Ketterling, R.P.
  • Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound
    Shaffer, L.G.; Rosenfeld, J.A.; Dabell, M.P.
  • Prenatal diagnosis of congenital heart defect by genome-wide high-resolution SNP array
    Liao, C.; Li, R.; Fu, F.
  • Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease
    Yan, Y.; Wu, Q.; Zhang, L.
  • Association of copy number variants with specific ultrasonographically detected fetal anomalies
    Donnelly, J.C.; Platt, L.D.; Rebarber, A.; Zachary, J.; Grobman, W.A.; Wapner, R.J.
  • Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis
    Jansen, F.A.R.; Blumenfeld, Y.J.; Fisher, A.
  • Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing
    Zhu, X.Y.; Li, J.; Ru, T.
  • Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis
    Sukenik-Halevy, R.; Sukenik, S.; Koifman, A.
  • Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis
    Du, L.; Xie, H.N.; Huang, L.H.; Xie, Y.J.; Wu, L.H.
  • Fetal right aortic arch: associated anomalies, genetic anomalies with chromosomal microarray analysis, and postnatal outcome
    Peng, R.; Xie, H.N.; Zheng, J.; Zhou, Y.; Lin, M.F.
  • The use of chromosomal microarray analysis in prenatal diagnosis. Committee opinion no. 581
  • National Birth Defects Prevention Study. Seeking causes: classifying and evaluating congenital heart defects in etiologic studies
    Botto, L.D.; Lin, A.E.; Riehle-Colarusso, T.; Malik, S.; Correa, A.
  • 1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation
    Hu, P.; Wang, Y.; Meng, L.L.
  • Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis
    Conlin, L.K.; Thiel, B.D.; Bonnemann, C.G.
  • Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges
    Sahoo, T.; Dzidic, N.; Strecker, M.N.
  • SgD-CNV, a database for common and rare copy number variants in three Asian populations
    Xu, H.Y.; Poh, W.T.; Sim, X.L.
  • The contribution of chromosomal abnormalities to congenital heart defects: a population-based study
    Hartman, R.J.; Rasmussen, S.A.; Botto, L.D.
  • Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis
    Grande, M.; Jansen, F.A.R.; Blumenfeld, Y.J.
  • Copy number variations with isolated fetal ventriculomegaly
    Hu, P.; Wang, Y.; Sun, R.
  • Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction
    Zhu, H.; Lin, S.; Huang, L.
  • Effect of copy number variants on outcomes for infants with single ventricle heart defects
    Carey, A.S.; Liang, L.; Edwards, J.