Literature DB >> 21210475

Screening for fetal aneuploidies at 11 to 13 weeks.

Kypros H Nicolaides1.   

Abstract

Effective screening for major aneuploidies can be provided in the first trimester of pregnancy. Screening by a combination of fetal nuchal translucency and maternal serum free-β-human chorionic gonadotrophin and pregnancy-associated plasma protein-A can identify about 90% of fetuses with trisomy 21 and other major aneuploidies for a false-positive rate of 5%. Improvement in the performance of first-trimester screening can be achieved by firstly, inclusion in the ultrasound examination assessment of the nasal bone and flow in the ductus venosus, hepatic artery and across the tricuspid valve, and secondly, carrying out the biochemical test at 9 to 10 weeks and the ultrasound scan at 12 weeks.
Copyright © 2011 John Wiley & Sons, Ltd.

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Year:  2011        PMID: 21210475     DOI: 10.1002/pd.2637

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  68 in total

Review 1.  Imaging clues in the prenatal diagnosis of syndromes and aneuploidy.

Authors:  Judy A Estroff
Journal:  Pediatr Radiol       Date:  2012-03-06

2.  Combined first trimester screen or noninvasive prenatal testing or both.

Authors:  Tony Yew Teck Tan
Journal:  Singapore Med J       Date:  2015-01       Impact factor: 1.858

3.  Attitudes of women of advanced maternal age undergoing invasive prenatal diagnosis and the impact of genetic counselling.

Authors:  Lea Godino; Eva Pompilii; Federica D'Anna; Antonio M Morselli-Labate; Elena Nardi; Marco Seri; Nicola Rizzo; Gianluigi Pilu; Daniela Turchetti
Journal:  Eur J Hum Genet       Date:  2015-05-27       Impact factor: 4.246

4.  Introducing the next generation sequencing in genomic amnio and villuos sampling. The so called "Next Generation Prenatal Diagnosis" (NGPD).

Authors:  Claudio Giorlandino; Alvaro Mesoraca; Domenico Bizzoco; Claudio Dello Russo; Antonella Cima; Gianluca Di Giacomo; Pietro Cignini; Francesco Padula; Nella Dugo; Laura D'Emidio; Cristiana Brizzi; Raffaella Raffio; Vincenzo Milite; Lucia Mangiafico; Claudio Coco; Ornella Carcioppolo; Roberto Vigna; Marialuisa Mastrandrea; Luisa Mobili
Journal:  J Prenat Med       Date:  2014 Jan-Mar

5.  Clinical Utility of Non-Invasive Prenatal Screening from Maternal Blood.

Authors:  Viorica Radoi; Camil Bohiltea; Roxana Bohiltea; Monica Cirstoiu
Journal:  Maedica (Bucur)       Date:  2015-09

Review 6.  Prenatal diagnosis of spina bifida: from intracranial translucency to intrauterine surgery.

Authors:  Waldo Sepulveda; Amy E Wong; Francisco Sepulveda; Juan L Alcalde; Juan C Devoto; Felipe Otayza
Journal:  Childs Nerv Syst       Date:  2017-06-07       Impact factor: 1.475

7.  The IONA® Test: Development of an Automated Cell-Free DNA-Based Screening Test for Fetal Trisomies 13, 18, and 21 That Employs the Ion Proton Semiconductor Sequencing Platform.

Authors:  Francesco Crea; Matthew Forman; Rachel Hulme; Robert W Old; Dan Ryan; Rosalyn Mazey; Michael D Risley
Journal:  Fetal Diagn Ther       Date:  2017-02-08       Impact factor: 2.587

8.  Risk Assessment at 11-14-Week Antenatal Visit: A Tertiary Referral Center Experience from South India.

Authors:  Anusha Vellamkondu; Akhila Vasudeva; Rajeshwari G Bhat; Asha Kamath; Sapna V Amin; Lavanya Rai; Pratap Kumar
Journal:  J Obstet Gynaecol India       Date:  2017-04-08

Review 9.  First Trimester Maternal Serum Screening Using Biochemical Markers PAPP-A and Free β-hCG for Down Syndrome, Patau Syndrome and Edward Syndrome.

Authors:  S Shiefa; M Amargandhi; J Bhupendra; S Moulali; T Kristine
Journal:  Indian J Clin Biochem       Date:  2012-10-12

10.  Down Syndrome - Genetics and Cardiogenetics.

Authors:  Vasilica Plaiasu
Journal:  Maedica (Bucur)       Date:  2017-09
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