Literature DB >> 28499534

Prenatal Diagnosis: Screening and Diagnostic Tools.

Laura M Carlson1, Neeta L Vora2.   

Abstract

The American Congress of Obstetricians and Gynecologists recommends that all pregnant women be offered aneuploidy screening or diagnostic testing. A myriad of screening and testing options are available to patients based on their risk profile and gestational age. Screening options include traditional serum analyte screening, such as first-trimester screening or quadruple screening, and more recently, cell-free DNA. Diagnostic testing choices include chorionic villus sampling and amniocentesis. The number of screening and diagnostic modalities complicates prenatal counseling for physicians and can be difficult for patients to grasp. Appropriate pretest and posttest counseling is important to ensure adequate understanding of results and ensure testing strategy is concordant with patient goals.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Amniocentesis; Aneuploidy; Cell-free DNA; Chorionic villus sampling; Genetic screening; Noninvasive prenatal screening

Mesh:

Year:  2017        PMID: 28499534      PMCID: PMC5548328          DOI: 10.1016/j.ogc.2017.02.004

Source DB:  PubMed          Journal:  Obstet Gynecol Clin North Am        ISSN: 0889-8545            Impact factor:   2.844


  34 in total

1.  A randomized trial of prenatal versus postnatal repair of myelomeningocele.

Authors:  N Scott Adzick; Elizabeth A Thom; Catherine Y Spong; John W Brock; Pamela K Burrows; Mark P Johnson; Lori J Howell; Jody A Farrell; Mary E Dabrowiak; Leslie N Sutton; Nalin Gupta; Noel B Tulipan; Mary E D'Alton; Diana L Farmer
Journal:  N Engl J Med       Date:  2011-02-09       Impact factor: 91.245

Review 2.  Committee Opinion No. 640: Cell-Free DNA Screening For Fetal Aneuploidy.

Authors: 
Journal:  Obstet Gynecol       Date:  2015-09       Impact factor: 7.661

3.  Maternal serum invasive trophoblast antigen (hyperglycosylated hCG) as a screening marker for Down syndrome during the second trimester.

Authors:  Glenn E Palomaki; Louis M Neveux; George J Knight; James E Haddow; Raj Pandian
Journal:  Clin Chem       Date:  2004-08-19       Impact factor: 8.327

4.  Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome.

Authors:  Giulia Maria Baffero; Edgardo Somigliana; Francesca Crovetto; Alessio Paffoni; Nicola Persico; Silvana Guerneri; Faustina Lalatta; Roberto Fogliani; Luigi Fedele
Journal:  Prenat Diagn       Date:  2012-09-07       Impact factor: 3.050

5.  Triple-marker test as screening for Down syndrome: a meta-analysis.

Authors:  A Conde-Agudelo; A C Kafury-Goeta
Journal:  Obstet Gynecol Surv       Date:  1998-06       Impact factor: 2.347

6.  Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy.

Authors:  K H Nicolaides; G Azar; D Byrne; C Mansur; K Marks
Journal:  BMJ       Date:  1992-04-04

7.  Practice Bulletin No. 162: Prenatal Diagnostic Testing for Genetic Disorders.

Authors: 
Journal:  Obstet Gynecol       Date:  2016-05       Impact factor: 7.661

8.  NIPT and Informed Consent: an Assessment of Patient Understanding of a Negative NIPT Result.

Authors:  Julie L Piechan; Karrie A Hines; Daniel L Koller; Kristyne Stone; Kimberly Quaid; Wilfredo Torres-Martinez; Divya Wilson Mathews; Tatiana Foroud; Lola Cook
Journal:  J Genet Couns       Date:  2016-04-01       Impact factor: 2.537

9.  The use of chromosomal microarray for prenatal diagnosis.

Authors:  Lorraine Dugoff; Mary E Norton; Jeffrey A Kuller
Journal:  Am J Obstet Gynecol       Date:  2016-07-15       Impact factor: 8.661

10.  Cell-free DNA vs sequential screening for the detection of fetal chromosomal abnormalities.

Authors:  Mary E Norton; Rebecca J Baer; Ronald J Wapner; Miriam Kuppermann; Laura L Jelliffe-Pawlowski; Robert J Currier
Journal:  Am J Obstet Gynecol       Date:  2015-12-18       Impact factor: 8.661

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  27 in total

1.  Prenatal diagnosis of thalassemia in 695 pedigrees from southeastern China: a 10-year follow-up study.

Authors:  Hailong Huang; Meihuan Chen; Lingji Chen; Min Zhang; Yan Wang; Na Lin; Liangpu Xu
Journal:  J Clin Lab Anal       Date:  2021-09-04       Impact factor: 2.352

2.  Factors causing timely referral for fetal echocardiography in the final diagnosis of congenital heart malformations: A cross-sectional study.

Authors:  Mojgan Barati; Nahal Nasehi; Sareh Aberoumand; Mahin Najafian; Abdolrahman Emami Moghadam
Journal:  Int J Reprod Biomed       Date:  2022-07-06

Review 3.  Nanostructures in non-invasive prenatal genetic screening.

Authors:  Samira Sadeghi; Mahdi Rahaie; Bita Ostad-Hasanzadeh
Journal:  Biomed Eng Lett       Date:  2021-10-11

Review 4.  Principles of and strategies for germline gene therapy.

Authors:  Don P Wolf; Paul A Mitalipov; Shoukhrat M Mitalipov
Journal:  Nat Med       Date:  2019-06-03       Impact factor: 53.440

5.  Rapid preimplantation genetic screening using a handheld, nanopore-based DNA sequencer.

Authors:  Shan Wei; Zachary R Weiss; Pallavi Gaur; Eric Forman; Zev Williams
Journal:  Fertil Steril       Date:  2018-10       Impact factor: 7.329

Review 6.  A narrative review of in utero gene therapy: advances, challenges, and future considerations.

Authors:  Nicholas K Yung; Nathan L Maassel; Sarah J Ullrich; Adele S Ricciardi; David H Stitelman
Journal:  Transl Pediatr       Date:  2021-05

7.  Multilevel regression modeling for aneuploidy classification and physical separation of maternal cell contamination facilitates the QF-PCR based analysis of common fetal aneuploidies.

Authors:  Predrag Noveski; Marija Terzic; Marija Vujovic; Maja Kuzmanovska; Emilija Sukarova Stefanovska; Dijana Plaseska-Karanfilska
Journal:  PLoS One       Date:  2019-08-20       Impact factor: 3.240

8.  Targeted fetal cell-free DNA screening for aneuploidies in 4,594 pregnancies: Single center study.

Authors:  Altug Koc; Ozge Ozer Kaya; Berk Ozyilmaz; Yasar B Kutbay; Ozgur Kirbiyik; Taha R Ozdemir; Kadri M Erdogan; Merve Saka Guvenc; Deniz C Oztekin; Mehmet Ozeren; Halil G Pala; Atalay Ekin; Cenk Gezer; Alkim G Sahingoz Yildirim; Bahar Konuralp Atakul; Secil Kurtulmus; Ugur Turhan; Cuneyt E Taner
Journal:  Mol Genet Genomic Med       Date:  2019-05-08       Impact factor: 2.183

Review 9.  Fetal gene therapy and pharmacotherapy to treat congenital hearing loss and vestibular dysfunction.

Authors:  Michelle L Hastings; John V Brigande
Journal:  Hear Res       Date:  2020-03-05       Impact factor: 3.208

10.  Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.

Authors:  Jinman Zhang; Xinhua Tang; Jilin Hu; Guilin He; Jian Wang; Yingting Zhu; Baosheng Zhu
Journal:  BMC Pregnancy Childbirth       Date:  2021-07-08       Impact factor: 3.007

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