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本文引用的文献

1
The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome.游离DNA筛查22q11.2缺失综合征的益处与局限性。
Prenat Diagn. 2017 Jan;37(1):53-60. doi: 10.1002/pd.4864. Epub 2016 Jul 25.
2
22q11.2 deletion syndrome.22q11.2 缺失综合征。
Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71.
3
Confined placental mosaicism and its impact on confirmation of NIPT results.局限性胎盘嵌合体及其对无创产前检测结果确认的影响。
Am J Med Genet C Semin Med Genet. 2016 Jun;172(2):118-22. doi: 10.1002/ajmg.c.31505. Epub 2016 May 17.
4
Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration.根据染色体异常情况,在绒毛活检和羊膜穿刺术之间做出基于循证的选择:阳性 NIPT 结果的细胞遗传学确认。
Expert Rev Mol Diagn. 2016;16(5):513-20. doi: 10.1586/14737159.2016.1152890. Epub 2016 Feb 29.
5
Cell-free DNA testing in a trisomy 21 pregnancy with confined placental mosaicism for a cell line with trisomy for both chromosomes 18 and 21.在一例21三体妊娠中进行游离DNA检测,该妊娠存在局限于胎盘的嵌合体,其中一个细胞系的18号和21号染色体均为三体。
Clin Case Rep. 2015 Nov 9;4(1):19-22. doi: 10.1002/ccr3.421. eCollection 2016 Jan.
6
Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis.使用游离DNA进行无创产前检测以检测唐氏、爱德华兹和帕陶氏综合征的准确性:一项系统评价和荟萃分析。
BMJ Open. 2016 Jan 18;6(1):e010002. doi: 10.1136/bmjopen-2015-010002.
7
Current controversies in prenatal diagnosis 1: should NIPT routinely include microdeletions/microduplications?产前诊断中的当前争议1:无创产前检测(NIPT)是否应常规包含微缺失/微重复检测?
Prenat Diagn. 2016 Jan;36(1):10-4. doi: 10.1002/pd.4710. Epub 2015 Nov 19.
8
Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.基于单核苷酸多态性的22q11.2缺失综合征无创产前筛查的临床经验。
Ultrasound Obstet Gynecol. 2016 Feb;47(2):177-83. doi: 10.1002/uog.15754. Epub 2016 Jan 5.
9
Committee Opinion Summary No. 640: Cell-Free DNA Screening For Fetal Aneuploidy.委员会意见摘要第640号:游离DNA筛查胎儿非整倍体
Obstet Gynecol. 2015 Sep;126(3):691-692. doi: 10.1097/01.AOG.0000471171.86798.ac.
10
Discordant circulating fetal DNA and subsequent cytogenetics reveal false negative, placental mosaic, and fetal mosaic cfDNA genotypes.不一致的循环胎儿DNA及后续细胞遗传学结果揭示了假阴性、胎盘嵌合及胎儿嵌合的游离胎儿DNA基因型。
J Transl Med. 2015 Aug 11;13:260. doi: 10.1186/s12967-015-0569-y.

22q11.2缺失的局限性胎盘嵌合体是无创产前检测(NIPT)结果不一致呈阳性的病因。

Confined placental mosaicism for 22q11.2 deletion as the etiology for discordant positive NIPT results.

作者信息

Bunnell M, Zhang C, Lee C, Bianchi D W, Wilkins-Haug L

机构信息

Maternal Fetal Medicine, Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, Boston, MA, USA.

Geisel School of Medicine at Dartmouth College, Hanover, NH, USA.

出版信息

Prenat Diagn. 2017 Apr;37(4):416-419. doi: 10.1002/pd.5022. Epub 2017 Mar 8.

DOI:10.1002/pd.5022
PMID:28198030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10131250/
Abstract

22q11.2 deletion, the most common microdeletion syndrome within the general population, is estimated to have a prevalence of 1 in 3000 to 6000. Non-invasive prenatal testing has recently expanded to include screening for several microdeletions including 22q11.2. Given the expansion of prenatal screening options to include microdeletions, it is important to understand the limits of this technology and the variety of reasons that a discordant positive result can occur. Here, we describe a case of a pregnant woman who received a positive non-invasive prenatal maternal plasma screen for 22q11.2 deletion. Maternal and postnatal neonatal peripheral blood cytogenetic, PCR, and fluorescence in situ hybridization studies were normal, but the placenta was mosaic for 22q11.2 deletion in two of three biopsy sites. This case illustrates both the complexities of pre- and post-test counseling for microdeletion screening and the potential for a discordant positive microdeletion result because of confined placental mosaicism. © 2017 John Wiley & Sons, Ltd.

摘要

22q11.2缺失是普通人群中最常见的微缺失综合征,据估计其患病率为1/3000至1/6000。非侵入性产前检测最近已扩展到包括对几种微缺失的筛查,其中就有22q11.2。鉴于产前筛查选项已扩展到包括微缺失,了解这项技术的局限性以及出现不一致阳性结果的各种原因很重要。在此,我们描述了一例孕妇,其非侵入性产前母体血浆筛查显示22q11.2缺失呈阳性。母体和产后新生儿外周血细胞遗传学、聚合酶链反应(PCR)及荧光原位杂交研究均正常,但胎盘在三个活检部位中的两个部位存在22q11.2缺失的嵌合体。该病例既说明了微缺失筛查的检测前和检测后咨询的复杂性,也显示了由于局限性胎盘嵌合体导致微缺失结果出现不一致阳性的可能性。© 2017约翰·威利父子有限公司