The Journal of Pediatrics
Volume 152, Issue 1 , Pages 20-24.e1, January 2008

Is Down Syndrome a Disappearing Birth Defect?

  • Veronica R. Collins, PhD

      Affiliations

    • From Public Health Genetics, Murdoch Childrens Research Institute, Royal Children’s Hospital, Victoria, Australia
    • Corresponding Author InformationReprint requests: Veronica Collins, PhD, Senior Research Officer, Public Health Genetics, Murdoch Childrens Research Institute, 10th Floor, Royal Children’s Hospital, Flemington Road, Parkville, VIC 3052, Australia.
  • ,
  • Evelyne E. Muggli, MPH

      Affiliations

    • From Public Health Genetics, Murdoch Childrens Research Institute, Royal Children’s Hospital, Victoria, Australia
  • ,
  • Merilyn Riley, B App Sci (HIM), Grad Dip (Epi & Biostats)

      Affiliations

    • Perinatal Data Collection Unit, Department of Human Services, Victoria, Australia.
  • ,
  • Sonia Palma, B App Sci (HIM)

      Affiliations

    • Perinatal Data Collection Unit, Department of Human Services, Victoria, Australia.
  • ,
  • Jane L. Halliday, PhD

      Affiliations

    • From Public Health Genetics, Murdoch Childrens Research Institute, Royal Children’s Hospital, Victoria, Australia
    • Perinatal Data Collection Unit, Department of Human Services, Victoria, Australia.

Received 22 February 2007; received in revised form 30 May 2007; accepted 25 July 2007. published online 22 October 2007.

Objective

To assess trends in the prevalence of Down syndrome (DS) from 1986 to 2004 in Victoria, Australia (population ∼5 million).

Study design

The Victorian Birth Defects Register and the Prenatal Diagnosis Database were linked to ascertain all cases of DS. Total and birth prevalence estimates were calculated per year and presented as 3-year moving averages.

Results

The total number of cases of DS increased from 113 in 1986 to 188 in 2004. The number of births declined over the first decade of the study, particularly in younger women, but total numbers have fluctuated between 45 and 60 births since 1996. In women under age 35 years, total prevalence was 10/10,000 until 1997 and then increased to 12.5/10,000. In older women, total prevalence increased from 70/10,000 to 90/10,000 in this time frame. Birth prevalence declined at first but remained relatively stable in the later years of the study. The proportion of cases diagnosed prenatally increased from 3% to 60% in younger women.

Conclusions

Our findings demonstrate the continuing need to devote resources to support individuals with DS and their families.

Abbreviations: BDR, Births Defects Register, DS, Down syndrome, PDCU, Perinatal Data Collection Unit

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 Supported by Australian National Health and Medical Research Council Research Fellowship 436904 (to J.H.).

PII: S0022-3476(07)00708-1

doi:10.1016/j.jpeds.2007.07.045

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The Journal of Pediatrics
Volume 152, Issue 1 , Pages 20-24.e1, January 2008