The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Trends in Down's syndrome live births and antenatal diagnoses in England and Wales from 1989 to 2008: analysis of data from the National Down Syndrome Cytogenetic Register
Open accessAbstract
OBJECTIVES: To describe trends in the numbers of Down's syndrome live births and antenatal diagnoses in England and Wales from 1989 to 2008. Design and setting The National Down Syndrome Cytogenetic Register holds details of 26488 antenatal and postnatal diagnoses of Down's syndrome made by all cytogenetic laboratories in England and Wales since 1989. INTERVENTIONS: Antenatal screening, diagnosis, and subsequent termination of Down's syndrome pregnancies. MAIN OUTCOME MEASURES: The number of live births with Down's syndrome. RESULTS: Despite the number of births in 1989/90 being similar to that in 2007/8, antenatal and postnatal diagnoses of Down's syndrome increased by 71% (from 1075 in 1989/90 to 1843 in 2007/8). However, numbers of live births with Down's syndrome fell by 1% (752 to 743; 1.10 to 1.08 per 1000 births) because of antenatal screening and subsequent terminations. In the absence of such screening, numbers of live births with Down's syndrome would have increased by 48% (from 959 to 1422), since couples are starting families at an older age. Among mothers aged 37 years and older, a consistent 70% of affected pregnancies were diagnosed antenatally. In younger mothers, the proportions of pregnancies diagnosed antenatally increased from 3% to 43% owing to improvements in the availability and sensitivity of screening tests. CONCLUSIONS: Since 1989, expansion of and improvements in antenatal screening have offset an increase in Down's syndrome resulting from rising maternal age. The proportion of antenatal diagnoses has increased most strikingly in younger women, whereas that in older women has stayed relatively constant. This trend suggests that, even with future improvements in screening, a large number of births with Down's syndrome are still likely, and that monitoring of the numbers of babies born with Down's syndrome is essential to ensure adequate provision for their needs.
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CUCKLE, H. S., WALD, N. J., & THOMPSON, S. G. (1987) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1987.tb03115.x · Cited by 604
Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection
Lo, Y. M. D., Tsui, N. B. Y., Chiu, R. W. K., Lau, T. K., Leung, T. N., Heung, M. M. S., Gerovassili, A., Jin, Y., Nicolaides, K. H., Cantor, C. R., et al. (2007) · Nature Medicine · doi:10.1038/nm1530 · Cited by 379
Revised estimates of the maternal age specific live birth prevalence of Down's syndrome
Morris, J. K., Mutton, D. E., & Alberman, E. (2002) · Journal of Medical Screening · doi:10.1136/jms.9.1.2 · Cited by 327
Self-citationEkelund, C. K., Jorgensen, F. S., Petersen, O. B., Sundberg, K., Tabor, A., & Danish Fetal Medicine Research Group (2008) · BMJ · doi:10.1136/bmj.a2547 · Cited by 311
Maternal age‐specific fetal loss rates in Down syndrome pregnancies
Savva, G. M., Morris, J. K., Mutton, D. E., & Alberman, E. (2006) · Prenatal Diagnosis · doi:10.1002/pd.1443 · Cited by 164
Self-citationCongenital anomaly surveillance in England—ascertainment deficiencies in the national system
Boyd, P. A., Armstrong, B., Dolk, H. M., Botting, B., Pattenden, S., Abramsky, L., Rankin, J. M., Vrijheid, M., & Wellesley, D. G. (2004) · BMJ · doi:10.1136/bmj.38300.665301.3a · Cited by 112
Is Down Syndrome a Disappearing Birth Defect?
Collins, V., Muggli, E., Riley, M. M., Palma, S., & Halliday, J. L. (2007) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2007.07.045 · Cited by 110
Cited by
Antonarakis, S. E., Skotko, B. G., Rafii, M. S., Strydom, A., Pape, S. E., Bianchi, D. W., Sherman, S. L., & Reeves, R. H. (2020) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0143-7 · Cited by 964
Synaptic Pathology of Down Syndrome
Garner, C. C., & Wetmore, D. Z. (2012) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-7091-0932-8_20 · Cited by 33
Metadata
- Authors
- Morris, J. K., & Alberman, E.
- Venue
- BMJ
- Publisher
- BMJ
- Published
- 2009-10-26
- Volume
- 339
- Issue
- oct26 3
- Pages
- b3794-b3794
- ISSN
- 0007-1447 (ISSN-L)
- 0959-8138
- 1468-5833
- OpenAlex
- W2126738653
- Cited by
- 293
- References
- 7
- FWCI
- 32.73
- Type
- journal article
- Language
- en
- Open access
- hybrid
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