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Decision to abort after a prenatal diagnosis of sex chromosome abnormality: a systematic review of the literature
Open accessAbstract
We performed a systematic review of factors affecting parental decisions to continue or terminate a pregnancy after prenatal diagnosis of a sex chromosome abnormality, as reported in published studies from 1987 to May 2011. Based on the Matrix Method for systematic reviews, 19 studies were found in five electronic databases, meeting specific inclusion/exclusion criteria. Abstracted data were organized in a matrix. Alongside the search for factors influencing parental decisions, each study was judged on its methodological quality and assigned a methodological quality score. Decisions either to terminate or to continue a sex chromosome abnormality-affected pregnancy shared five similar factors: specific type of sex chromosome abnormality, gestational week at diagnosis, parents' age, providers' genetic expertise, and number of children/desire for (more) children. Factors unique to termination decisions included parents' fear/anxiety and directive counseling. Factors uniquely associated with continuation decisions were parents' socioeconomic status and ethnicity. The studies' average methodological quality score was 10.6 (SD = 1.67; range, 8-14). Findings from this review can be useful in adapting and modifying guidelines for genetic counseling after prenatal diagnosis of a sex chromosome abnormality. Moreover, improving the quality of future studies on this topic may allow clearer understanding of the most influential factors affecting parental decisions.
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“In countries where termination of pregnancy is allowed, rates of termination of pregnancy following prenatal diagnosis of TS vary between 15.4% and 100%.59,81,82”
From Clinical practice guidelines for the care of girls and women with Turner syndrome. (2024) · cites this paper as [81]
Experimental — accuracy not yet measuredIn the citing paper
“Several factors have been found to influence the prospective parents’ decision to continue or terminate a pregnancy with a TS fetus.”
From Clinical practice guidelines for the care of girls and women with Turner syndrome. (2024) · cites this paper as [81]
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Cites
Long term outcome in children of sex chromosome abnormalities
Ratcliffe, S. G. (1999) · Archives of Disease in Childhood · doi:10.1136/adc.80.2.192 · Cited by 334
Suther, S., & Goodson, P. (2003) · Genetics in Medicine · doi:10.1097/01.gim.0000055201.16487.61 · Cited by 264
Self-citationBateson, M. C. (2004) · PubMed Central · Cited by 199
Variation in the decision to terminate pregnancy in the setting of fetal aneuploidy
Shaffer, B. L., Caughey, A. B., & Norton, M. E. (2006) · Prenatal Diagnosis · doi:10.1002/pd.1462 · Cited by 192
Marteau, T. M., Drake, H., & Bobrow, M. (1994) · Journal of Medical Genetics · doi:10.1136/jmg.31.11.864 · Cited by 174
Holmes-Siedle, M., Ryynänen, M., & Lindenbaum, R. H. (1987) · Prenatal Diagnosis · doi:10.1002/pd.1970070403 · Cited by 164
Parental decision following prenatal diagnosis of fetal chromosome abnormality
Verp, M. S., Bombard, A. T., Simpson, J. L., Elias, S., Reynolds, J. F., & Hall, J. G. (1988) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320290320 · Cited by 159
Genetic counseling for sex chromosome abnormalities
Linden, M. G., Bender, B. G., & Robinson, A. (2002) · American Journal of Medical Genetics · doi:10.1002/ajmg.10391 · Cited by 159
Fifty‐one prenatally diagnosed children and adolescents with sex chromosome abnormalities
Linden, M. G., & Bender, B. G. (2002) · American Journal of Medical Genetics · doi:10.1002/ajmg.10394 · Cited by 149
Decision-making for termination of pregnancies with fetal anomalies: analysis of 53,000 pregnancies
Schechtman, K. B. (2002) · Obstetrics and Gynecology · doi:10.1016/s0029-7844(01)01673-8 · Cited by 144
Research works printed but not linked: 1
- Garrard J. Health Sciences Literature Review Made Easy: The Matrix Method, 2nd edn. Jones and Bartlett Publishers: Sudbury, MA, 2006.
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on behalf of the European Society of Human Genetics (ESHG) and the American Society of Human Genetics (ASHG), Dondorp, W., de Wert, G. M. W. R., Bombard, Y., Bianchi, D. W., Bergmann, C., Borry, P., Chitty, L. S., Fellmann, F., Forzano, F., et al. (2015) · European Journal of Human Genetics · doi:10.1038/ejhg.2015.57 · Cited by 347
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Clinical practice guidelines for the care of girls and women with Turner syndrome.
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Viuff, M. H., Stochholm, K., Uldbjerg, N., Nielsen, B. B., the Danish Fetal Medicine Study Group, & Gravholt, C. H. (2015) · Human Reproduction · doi:10.1093/humrep/dev192 · Cited by 78
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Self-citationHooks, J., Wolfberg, A., Wang, E. T., Struble, C. A., Zahn, J. M., Juneau, K., Mohseni, M., Huang, S., Bogard, P. E., Song, K., et al. (2014) · Prenatal Diagnosis · doi:10.1002/pd.4338 · Cited by 60
Jacobs, M., Cooper, S., McGowan, R., Nelson, S. M., & Pell, J. P. (2016) · PLoS ONE · doi:10.1371/journal.pone.0166909 · Cited by 58
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Deng, C., Cheung, S. W., & Liu, H. (2021) · Expert Review of Molecular Diagnostics · doi:10.1080/14737159.2021.1911651 · Cited by 31
Bowman‐Smart, H., Gyngell, C., Mand, C., Amor, D. J., Delatycki, M. B., & Savulescu, J. (2021) · The American Journal of Bioethics · doi:10.1080/15265161.2021.1996659 · Cited by 33
Autism and social anxiety in children with sex chromosome trisomies: an observational study
Wilson, A. C., King, J., & Bishop, D. (2019) · Wellcome Open Research · doi:10.12688/wellcomeopenres.15095.1 · Cited by 28
Loughry, L., Pynaker, C., White, M., Halliday, J. L., & Hui, L. (2022) · Prenatal Diagnosis · doi:10.1002/pd.6103 · Cited by 28
Lau, T. K., Chan, M. K., Lo, P. S. S., Chan, H. Y. C., Chan, W. K., Koo, T. Y., Ng, H. Y. J., & Pooh, R. K. (2012) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.3109/14767058.2012.712569 · Cited by 28
Bussolaro, S., Raymond, Y. C., Acreman, M. L., Guido, M., Costa, F. D. S., Rolnik, D. L., & Fantasia, I. (2022) · American Journal of Obstetrics & Gynecology MFM · doi:10.1016/j.ajogmf.2022.100844 · Cited by 29
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Parham, L., Michie, M., & Allyse, M. A. (2017) · Current Genetic Medicine Reports · doi:10.1007/s40142-017-0113-x · Cited by 22
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Jeon, K. C., Chen, L., & Goodson, P. (2012) · Genetics in Medicine · doi:10.1038/gim.2012.33 · Cited by 1
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Gardner, R. J. M., & Amor, D. J. (2018) · Oxford University Press eBooks · doi:10.1093/med/9780199329007.003.0013
Complex Chromosomal Rearrangements
Gardner, R. J. M., & Amor, D. J. (2018) · Oxford University Press eBooks · doi:10.1093/med/9780199329007.003.0010
Metadata
- Authors
- Jeon, K. C., Chen, L.-S., & Goodson, P.
- Affiliations
- Texas A&M University (US)
- Corresponding author
- Jeon, Kwon Chan
- Venue
- Genetics in Medicine
- Publisher
- Elsevier BV
- Published
- 2012-01
- Volume
- 14
- Issue
- 1
- Pages
- 27-38
- ISSN
- 1098-3600 (ISSN-L)
- OpenAlex
- W2091333572
- Cited by
- 139
- References
- 39
- Citations by year
- 2026: 3 · 2025: 21 · 2024: 10 · 2023: 4 · 2022: 13 · 2021: 7 · 2020: 5 · 2019: 7 · 2018: 37 · 2017: 2 · 2016: 4 · 2015: 8 · 2014: 4 · 2013: 6 · 2012: 7
- FWCI
- 1.25
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Genetics in Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Prenatal Screening and Diagnostics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Ethics and Legal Issues in Pediatric Healthcare
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Sexual Differentiation and Disorders
- Keywords
- sex chromosome abnormalities, prenatal diagnosis, abortion, continuation of pregnancy, parental decision-making, genetic counseling, gestational age at diagnosis, parental age, socioeconomic status, ethnicity, fear and anxiety, desire for more children
- MeSH terms
- Abortion, Induced, Decision Making, Female, Humans, Parents, Pregnancy, Pregnancy Outcome, Prenatal Diagnosis, Sex Chromosome Aberrations
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