Literature DB >> 27126496

Live births, natural losses, and elective terminations with Down syndrome in Massachusetts.

Gert de Graaf1, Frank Buckley2,3, Brian G Skotko4,5.   

Abstract

PURPOSE: No studies to date have reported an estimated number of live births, elective terminations, and natural losses (miscarriages and stillbirths) for Down syndrome (DS) in Massachusetts (MA). These numbers would be helpful to estimate how many expectant parents of children with DS need support and the number of live-born children with DS who require services.
METHODS: Combining robust data sets, including the Annual Reports of the MA Birth Defects Monitoring Program, we estimated the number of live births, elective terminations, and natural losses with Down syndrome from 1900 to 2010.
RESULTS: The live birth prevalence for DS in MA for the most recent years for which data are available (2006-2010) was estimated at 12.4 per 10,000 live births, with a total of approximately 94 live births annually. During this period, an estimated 126 DS-related elective pregnancy terminations were performed in MA annually. As of 2008, the estimated rate at which live births with DS was reduced as a consequence of DS-related elective pregnancy terminations was 49%.
CONCLUSION: The reduction of live births with DS is significantly higher in MA than in the rest of the United States as a whole. However, ethnic and racial differences in reduction rates were similar-highest for Asians/Pacific Islanders, followed by non-Hispanic whites, non-Hispanic blacks/Africans, and Hispanics.Genet Med 18 5, 459-466.

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Year:  2016        PMID: 27126496     DOI: 10.1038/gim.2016.15

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  25 in total

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Authors:  B Khoshnood; P Pryde; S Wall; J Singh; R Mittendorf; K S Lee
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Journal:  Hum Biol       Date:  2003-08       Impact factor: 0.553

4.  Maternal age specific risk rate estimates for Down syndrome among live births in whites and other races from Ohio and metropolitan Atlanta, 1970-1989.

Authors:  C A Huether; J Ivanovich; B S Goodwin; E L Krivchenia; V S Hertzberg; L D Edmonds; D S May; J H Priest
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318

5.  The effects of prenatal diagnosis, population ageing, and changing fertility rates on the live birth prevalence of Down syndrome in New York State, 1983-1992.

Authors:  C L Olsen; P K Cross; L J Gensburg; J P Hughes
Journal:  Prenat Diagn       Date:  1996-11       Impact factor: 3.050

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9.  Maternal age-specific Down syndrome rates by maternal race/ethnicity, Hawaii, 1986-2000.

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Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2008-03-28       Impact factor: 5.747

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5.  The role of information provision in economic evaluations of non-invasive prenatal testing: a systematic review.

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7.  Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus.

Authors:  Jonathan D Santoro; Lina Patel; Ryan Kammeyer; Robyn A Filipink; Grace Y Gombolay; Kathleen M Cardinale; Diego Real de Asua; Shahid Zaman; Stephanie L Santoro; Sammer M Marzouk; Mellad Khoshnood; Benjamin N Vogel; Runi Tanna; Dania Pagarkar; Sofia Dhanani; Maria Del Carmen Ortega; Rebecca Partridge; Maria A Stanley; Jessica S Sanders; Alison Christy; Elise M Sannar; Ruth Brown; Andrew A McCormick; Heather Van Mater; Cathy Franklin; Gordon Worley; Eileen A Quinn; George T Capone; Brian Chicoine; Brian G Skotko; Michael S Rafii
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8.  Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.

Authors:  Anthony R Gregg; Brian G Skotko; Judith L Benkendorf; Kristin G Monaghan; Komal Bajaj; Robert G Best; Susan Klugman; Michael S Watson
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Review 9.  Rodent models in Down syndrome research: impact and future opportunities.

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