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Journal of Obstetrics and Gynaecology Volume 38, 2018 - Issue 4
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Original Article

What would be missed in the first trimester if nuchal translucency measurement is replaced by cell free DNA foetal aneuploidy screening?

Lv-Yin HuangPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China
,
Min PanPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China
,
Jin HanPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China
,
Li ZhenPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China
,
Xin YangPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, China
&
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, ChinaCorrespondence[email protected]
Pages 498-501 | Received 07 Jun 2017, Accepted 03 Sep 2017, Published online: 12 Feb 2018

Citations (12)

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Read on this site (1)

Xin-Rong Zhao, Li Gao, Yi Wu & Yan-Lin Wang. (2020) Application of chromosomal microarray in fetuses with increased nuchal translucency. The Journal of Maternal-Fetal & Neonatal Medicine 33:10, pages 1749-1754.
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Articles from other publishers (11)

Yong Xu, Siqi Hu, Liyuan Chen, Ying Hao, Hu Zhang, Zhiyong Xu, Weiqing Wu & Liyanyan Deng. (2023) Application of non-invasive prenatal testing in screening chromosomal aberrations in pregnancies with different nuchal translucency cutoffs. Molecular Cytogenetics 16:1.
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Sangeeta Khatter, Meena Lall, Shruti Agrawal, Sunita Bijarnia Mahay, Nandita Dimri, Nidhish Sharma, Kanwal Gujral, Ishwar C. Verma & Ratna D. Puri. (2023) The Impact of Isolated Increased Nuchal Translucency ≥95th Centile on Perinatal Outcome: A Prospective Cohort Study from a North Indian Genetic Center. Journal of Fetal Medicine 10:01, pages 009-015.
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Beiyi Lu, Lizhong Yin, Jing Wang, Bin Yu & Bin Zhang. (2023) Residual risk of noninvasive prenatal screening in pregnancies with ultrasound anomalies. Journal of Gynecology Obstetrics and Human Reproduction 52:1, pages 102515.
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Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, Laura Bernardini, Antonella Giancotti, Gerardo Piacentini, Alessandro De Luca & Antonio Pizzuti. (2022) A Pain in the Neck: Lessons Learnt from Genetic Testing in Fetuses Detected with Nuchal Fluid Collections, Increased Nuchal Translucency versus Cystic Hygroma—Systematic Review of the Literature, Meta-Analysis and Case Series. Diagnostics 13:1, pages 48.
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Adena Bargad & Hannah VogtSchaller. 2022. Pediatric Diagnostic Labs for Primary Care: An Evidence-based Approach. Pediatric Diagnostic Labs for Primary Care: An Evidence-based Approach 29 65 .
Lena Sagi-Dain, Amihood Singer, Reeval Segel, Racheli Berger, Bibi Kanengisser-Pines & Idit Maya. (2021) The yield of chromosomal microarray in pregnancies with congenital cardiac defects and normal noninvasive prenatal screening. American Journal of Obstetrics and Gynecology 225:3, pages 333.e1-333.e14.
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Daniel Kane, Mary E. D’Alton & Fergal D. Malone. (2021) Rare chromosomal abnormalities: Can they be identified using conventional first trimester combined screening methods?. European Journal of Obstetrics & Gynecology and Reproductive Biology: X 10, pages 100123.
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Lena Sagi-Dain, Amihood Singer, Shay Ben Shachar, Sagi Josefsberg Ben Yehoshua, Michal Feingold-Zadok, Lior Greenbaum & Idit Maya. (2021) Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mm. Obstetrics & Gynecology 137:1, pages 126-131.
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Dongsook Lee, Sanghee Go, Sohyun Na, Surim Park, Jinyoung Ma & Doyeong Hwang. (2020) Clinical application of chromosomal microarray for pathogenic genomic imbalance in fetuses with increased nuchal translucency but normal karyotype. Journal of Genetic Medicine 17:1, pages 21-26.
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J. Miranda, F. Paz y Miño, V. Borobio, C. Badenas, L. Rodriguez‐Revenga, M. Pauta & A. Borrell. (2020) Should cell‐free DNA testing be used in pregnancy with increased fetal nuchal translucency? . Ultrasound in Obstetrics & Gynecology 55:5, pages 645-651.
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Iris Holzer, Peter W. Husslein, Dieter Bettelheim, Julia Scheidl, Herbert Kiss & Alex Farr. (2019) Value of increased nuchal translucency in the era of noninvasive prenatal testing with cell‐free DNA . International Journal of Gynecology & Obstetrics 145:3, pages 319-323.
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