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Sidorchuk M.A.

National Medical Research Center for Obstetrics, Gynecology and Perinatology named after academician V.I. Kulakov

Everything will be fine!

Authors:

Sidorchuk M.A.

More about the authors

Journal: Non Nocere. New Therapeutic Journal. 2026;(3): 28‑31

Read: 91 times

To cite this article:

Sidorchuk MA. Everything will be fine! Non Nocere. New Therapeutic Journal. 2026;(3):28‑31. (In Russ.)

References:

  1. Kagan KO, Sonek J, Wagner P, Hoopmann M. Principles of first trimester screening in the age of non-invasive prenatal diagnosis: screening for chromosomal abnormalities. Arch Gynecol Obstet. 2017 Oct;296(4):645-651.  https://doi.org/10.1007/s00404-017-4459-9
  2. Kagan KO, Etchegaray A, Zhou Y, Wright D, Nicolaides KH. Prospective validation of first-trimester combined screening for trisomy 21. Ultrasound Obstet Gynecol. 2009 Jul;34(1):14-18.  https://doi.org/10.1002/uog.6412
  3. Abedalthagafi M, Bawazeer S, Fawaz RI, Heritage AM, Alajaji NM, Faqeih E. Non-invasive prenatal testing: a revolutionary journey in prenatal testing. Front Med (Lausanne). 2023 Nov 9;10:1265090. https://doi.org/10.3389/fmed.2023.1265090
  4. Sukhikh G.T., Trofimov D.Yu., Barkov I.Yu., et al. Methodological recommendations “Noninvasive prenatal screening (NIPS) for fetal aneuploidies in maternal blood by high-throughput sequencing (NGS)”. Akusherstvo i Ginekologiya/Obstetrics and Gynecology. 2024; (3) (Supplement): 4-24. (In Russ.) https://doi.org/10.18565/aig.2024.51
  5. Tarasenko O.A., Vashukova E.S., Kozyulina P.Yu., et al. Experience of using high-throughput sequencing (NGS) for noninvasive prenatal screening of fetal aneuploidy at the D.O. Ott Research Institute of Obstetrics, Gynecology and Reproduction. Akusherstvo i Ginekologiya /Obstetrics and Gynecology. 2022; 10: 37-49. (In Russ.) https://doi.org/10.18565/aig.2022.10.37-49
  6. Luo W, He B, Han D, et al. A new contingent screening strategy increased detection rate of trisomy 21 in the first trimester. BMC Pregnancy Childbirth. 2023 Nov 14;23(1):791.  https://doi.org/10.1186/s12884-023-06115-1
  7. Kagan KO, Avgidou K, Molina FS, Gajewska K, Nicolaides KH. Relation between increased fetal nuchal translucency thickness and chromosomal defects. Obstet Gynecol. 2006 Jan;107(1):6-10.  https://doi.org/10.1097/01.AOG.0000191301.63871.c6
  8. Timmerman E, Pajkrt E, Maas SM, Bilardo CM. Enlarged nuchal translucency in chromosomally normal fetuses: strong association with orofacial clefts. Ultrasound Obstet Gynecol. 2010 Oct;36(4):427-432.  https://doi.org/10.1002/uog.7650
  9. Bardi F, Bosschieter P, Verheij J, et al. Is there still a role for nuchal translucency measurement in the changing paradigm of first trimester screening? Prenat Diagn. 2020 Jan;40(2):197-205.  https://doi.org/10.1002/pd.5590
  10. Salomon LJ, Alfirevic Z, Audibert F, et al. ISUOG Clinical Standards Committee. ISUOG consensus statement on the impact of non-invasive prenatal testing (NIPT) on prenatal ultrasound practice. Ultrasound Obstet Gynecol. 2014 Jul;44(1):122-123.  https://doi.org/10.1002/uog.13393
  11. Kalashnikova E.A., Glotov A.S., Andreyeva E.N., Barkov I.Y., Bobrovnik G.Y., Dubrovina E.V., Zhuchenko L.A. Current relevance of non-invasive prenatal study of cell-free fetal DNA in the mother’s blood and prospects for its application in mass screening of pregnant women in the Russian Federation. Journal of obstetrics and women’s diseases. 2021;70(1):19-50.  https://doi.org/10.17816/JOWD56573

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