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The Journal of Maternal-Fetal & Neonatal Medicine Volume 30, 2017 - Issue 8
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Short Report

How necessary is to analyze PTPN11 gene in fetuses with first trimester cystic hygroma and normal karyotype?

Alper Gezdirici1 Department of Medical Genetics, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey and Correspondence[email protected]
,
Ali Ekiz2 Department of Maternal Fetal Medicine, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey
,
Elif Yılmaz Güleç1 Department of Medical Genetics, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey and
,
Başak Kaya2 Department of Maternal Fetal Medicine, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey
,
Salim Sezer2 Department of Maternal Fetal Medicine, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey
&
Alev Atış Aydın2 Department of Maternal Fetal Medicine, Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey
Pages 938-941 | Received 24 Dec 2015, Accepted 16 May 2016, Published online: 08 Jun 2016

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David M Sherer, Vicky Hsieh, Anika Hall, Allison Gerren, Erin Walters & Mudar Dalloul. (2022) Current Perspectives of Prenatal Cell-free DNA Screening in Clinical Management of First-Trimester Septated Cystic Hygroma. International Journal of Women's Health 14, pages 1499-1518.
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Articles from other publishers (12)

Wei Jian, Huizhen Yuan, Yu Liu, Jimei Sun, Fei Chen, Yufan Li & Min Chen. (2023) Prenatal diagnosis of Noonan syndrome in a set of monozygotic twins- a case report. BMC Pregnancy and Childbirth 23:1.
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Joseph J. Maleszewski, Allen P. Burke, John P. Veinot & William D. Edwards. 2023. Disorders of the Heart and Blood Vessels. Disorders of the Heart and Blood Vessels 623 648 .
Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki & Samira Kalayinia. (2022) A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects. European Journal of Medical Research 27:1.
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Rafael Eduardo Tarazona-Bueno, Rafael Leonardo Aragón-Mendoza, Deisy Yurany Daza Leguizamón & Marcela Altman-Restrepo. (2022) Perinatal prognosis in euploid fetus with cystic hygroma. Report of two clinical cases. Case reports 8:2.
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Meiying CaiNan GuoNa LinHailong HuangLiangpu Xu. (2022) Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study. Medicine 101:47, pages e31689.
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Chih-Ping Chen, Shin-Wen Chen, Fang-Tzu Wu, Yen-Ting Pan & Wayseen Wang. (2022) Spontaneous resolution of septated cystic hygroma with a severely increased nuchal translucency thickness of 5.8 mm detected in the first-trimester in a pregnancy with no abnormalities in chromosomal, microarray and whole exome sequencing analyses and a favorable fetal outcome. Taiwanese Journal of Obstetrics and Gynecology 61:6, pages 1088-1089.
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Chih-Ping Chen. (2022) Prenatal diagnosis of euploid increased nuchal translucency on fetal ultrasound (I): Noonan syndrome: Prenatal diagnosis and genetic testing. Journal of Medical Ultrasound 30:4, pages 257.
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David M. Sherer, Vicky Hsieh, Mila Kheyman, Olabisi Makanjuola & Mudar Dalloul. (2021) Cell-free DNA screening following first-trimester septated cystic hygroma leading to diagnosis of previously unknown familial Noonan syndrome. European Journal of Obstetrics & Gynecology and Reproductive Biology 264, pages 389.
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Aubrey Milunsky & Jeff M. MilunskyJeff M. Milunsky. 2021. Genetic Disorders and the Fetus. Genetic Disorders and the Fetus 572 610 .
I. AlmonacidP. ZuletaC. NeriA. ZanninM. GarzónJ. DoradoF. Medina & L.G. Celis. (2020) CYSTIC HYGROMA AND THE IMPORTANCE OF THE PRENATAL DIAGNOSIS: ABOUT A CASE. Journal of Basic and Applied Genetics 31:Issue 2, pages 39-44.
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Lore Schreurs, Lore Lannoo, Luc De Catte, Dominique Van Schoubroeck, Koenraad Devriendt & Jute Richter. (2018) First trimester cystic hygroma colli: Retrospective analysis in a tertiary center. European Journal of Obstetrics & Gynecology and Reproductive Biology 231, pages 60-64.
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Marwan M. Ali, Stephen T. Chasen & Mary E. Norton. (2017) Testing for Noonan syndrome after increased nuchal translucency. Prenatal Diagnosis 37:8, pages 750-753.
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