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ISRN Obstetrics and Gynecology
Volume 2012 (2012), Article ID 524537, 7 pages
Why Do Parents Prefer to Know the Fetal Sex as Part of Invasive Prenatal Testing?
1Department of Human Genetics, Nijmegen Medical Centre, Radboud University Nijmegen,
6500 HB Nijmegen, The Netherlands
2Department of Obstetrics and Gynaecology, Nijmegen Medical Centre, Radboud University Nijmegen, 6500 HB Nijmegen, The Netherlands
3Department of Obstetrics and Gynaecology, Erasmus MC, University Medical Centre Rotterdam, 3015 GE Rotterdam, The Netherlands
4Department of Epidemiology, Biostatistics and HTA, Nijmegen Medical Centre, Radboud University Nijmegen, 6500 HB Nijmegen, The Netherlands
5Obstetrics and Gynaecology, Rijnstate Hospital, 6815 AD Arnhem, The Netherlands
6Obstetrics and Gynaecology, Jeroen Bosch Hospital, 5200 ME ‘s-Hertogenbosch, The Netherlands
7Obstetrics and Gynaecology, Medical Spectrum Twente, 7500 KA Enschede, The Netherlands
8Obstetrics and Gynaecology, St. Elisabeth Hospital, 5022 GC Tilburg, The Netherlands
Received 10 October 2012; Accepted 14 November 2012
Academic Editors: R. Kimmig and P. G. Larsson
Copyright © 2012 Angelique J. A. Kooper et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- R. W. K. Chiu and Y. M. D. Lo, “Application of fetal DNA in maternal plasma for noninvasive prenatal diagnosis,” Expert Review of Molecular Diagnostics, vol. 2, no. 1, pp. 32–40, 2002.
- R. J. P. Rijnders, G. C. M. L. Christiaens, B. Bossers, J. J. van der Smagt, C. E. van der Schoot, and M. De Haas, “Clinical applications of cell-free fetal DNA from maternal plasma,” Obstetrics and Gynecology, vol. 103, no. 1, pp. 157–164, 2004.
- R. J. Rijnders, C. E. van der Schoot, B. Bossers, M. A. de Vroede, and G. C. Christiaens, “Fetal sex determination from maternal plasma in pregnancies at risk for Congenital Adrenal Hyperplasia,” Obstetrics & Gynecology, vol. 98, no. 3, pp. 374–378, 2001.
- M. G. Linden and B. G. Bender, “Genetic counseling for sex chromosome abnormalities,” American Journal of Medical Genetics, vol. 110, no. 1, pp. 3–10, 2002.
- E. García, D. R. M. Timmermans, and E. van Leeuwen, “Rethinking autonomy in the context of prenatal screening decision-making,” Prenatal Diagnosis, vol. 28, no. 2, pp. 115–120, 2008.
- P. A. Boyd, M. Loane, E. Garne, B. Khoshnood, and H. Dolk, “Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancy,” European Journal of Human Genetics, vol. 19, no. 2, pp. 231–234, 2011.
- RIVM (Dutch National Institute for Public Health and the Environment), “A brief history of the 20-week ultrasound,” 2009, http://www.rivm.nl/pns.
- K. Harrington, V. Armstrong, J. Freeman, J. Aquilina, and S. Campbell, “Fetal sexing by ultrasound in the second trimester: Maternal preference and professional ability,” Ultrasound in Obstetrics and Gynecology, vol. 8, no. 5, pp. 318–321, 1996.
- S. Meagher and G. Davison, “Early second-trimester determination of fetal gender by ultrasound,” Ultrasound in Obstetrics and Gynecology, vol. 8, no. 5, pp. 322–324, 1996.
- M. Odeh, V. Granin, M. Kais, E. Ophir, and J. Bornstein, “Sonographic fetal gender determination,” Obstetrical & Gynecological Survey, vol. 64, pp. 50–57, 2009.
- E. S. Bauman, L. N. Hollander, D. E. V. Fauchon, A. J. Eggink, F. K. Lotgering, and R. J. Benzie, “What factors are associated with parental desire to find out the sex of their baby?” ASUM Ultrasound Bulletin, vol. 11, pp. 19–24, 2008.
- T. D. Shipp, D. Z. Shipp, B. Bromley et al., “What factors are associated with parents' desire to know the sex of their unborn child?” Birth, vol. 31, no. 4, pp. 272–279, 2004.
- K. Hank and H. P. Kohler, “Gender preferences for children in Europe: empirical results from 17 FFS countries,” Demographic Research, vol. 2, no. 1, 2000.
- Fest, “Prenatal sex selection: a closed ethical discussion?” Erasmus Journal of Medicine, vol. 2, no. 1, 2011.
- R. Jacobsen, H. Molier, and G. Engholm, “Fertility rates in Denmark in relation to the sexes of preceding children in the family,” Human Reproduction, vol. 14, no. 4, pp. 1127–1130, 1999.
- J. J. P. M. Pieters, A. J. A. Kooper, A. Geurts van Kessel, D. D. M. Braat, and A. P. T. Smits, “Incidental prenatal diagnosis of sex chromosome aneuploidies: health, behavior and fertility,” ISRN Obstetrics and Gynecology, vol. 2011, Article ID 807106, 10 pages, 2011.
- M. C. van Zwieten, D. L. Willems, L. L. Litjens, H. G. Schuring-Blom, and N. Leschot, “How unexpected are unexpected findings in prenatal cytogenetic diagnosis? a literature review,” European Journal of Obstetrics & Gynecology and Reproductive Biology, vol. 1, no. 120, pp. 15–21, 2005.
- G. Mezei, C. Papp, E. Tóth-Pál, A. Beke, and Z. Papp, “Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidy,” Obstetrics & Gynecology, vol. 104, pp. 94–101, 2004.