Selected birth defects data from population-based birth defects surveillance programs in the United States, 2006 to 2010: featuring trisomy conditions.

نویسندگان

  • Cara T Mai
  • James E Kucik
  • Jennifer Isenburg
  • Marcia L Feldkamp
  • Lisa K Marengo
  • Erin M Bugenske
  • Phoebe G Thorpe
  • Jodi M Jackson
  • Adolfo Correa
  • Russel Rickard
  • C J Alverson
  • Russell S Kirby
چکیده

The annual National Birth Defects Prevention Network (NBDPN) Congenital Malformations Surveillance Report includes state-level data on major birth defects (i.e., conditions present at birth that cause adverse structural changes in one or more parts of the body) and a directory of population-based birth defects surveillance systems in the United States. Beginning in 2012, these annually updated data and directory information are available in an electronic format accompanied by a data brief. This year’s report includes data from 41 population-based birth defects surveillance programs and a data brief highlighting the more common trisomy conditions (i.e., disorders characterized by an additional chromosome): trisomy 21 (commonly referred to as Down syndrome), trisomy 18, and trisomy 13.

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منابع مشابه

Public Health Practice of Population-Based Birth Defects Surveillance Programs in the United States.

CONTEXT Birth defects remain a leading cause of infant mortality in the United States and contribute substantially to health care costs and lifelong disabilities. State population-based surveillance systems have been established to monitor birth defects, yet no recent systematic examination of their efforts in the United States has been conducted. OBJECTIVE To understand the current populatio...

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Selected birth defects data from population-based birth defects surveillance programs in the United States, 2005–2009: Featuring critical congenital heart defects targeted for pulse oximetry screening.

Cara T. Mai,* Tiffany Riehle-Colarusso, Alissa O’Halloran, Janet D. Cragan, Richard S. Olney, Angela Lin, Marcia Feldkamp, Lorenzo D. Botto, Russel Rickard, Marlene Anderka, Mary Ethen, Carol Stanton, Joan Ehrhardt, and Mark Canfield, for the National Birth Defects Prevention Network National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atl...

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Development and implementation of the first national data quality standards for population-based birth defects surveillance programs in the United States

BACKGROUND Population-based birth defects surveillance is a core public health activity in the United States (U.S.); however, the lack of national data quality standards has limited the use of birth defects surveillance data across state programs. Development of national standards will facilitate data aggregation and utilization across birth defects surveillance programs in the U.S. METHODS B...

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Surveillance for and comparison of birth defect prevalences in two geographic areas--United States, 1983-88.

PROBLEM/CONDITION CDC and a number of states have developed surveillance systems to monitor the birth prevalence of major defects. REPORTING PERIOD COVERED This report covers birth defects surveillance in Metropolitan Atlanta, Georgia and selected jurisdictions in California for the years 1983-1988. DESCRIPTION OF SYSTEM The California Birth Defects Monitoring Program and the Metropolitan A...

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Collection, use, and protection of population-based birth defects surveillance data in the united states.

Birth defects surveillance systems collect population-based birth defects data from multiple sources to track trends in prevalence, identify risk factors, refer affected families to services, and evaluate prevention efforts. Strong state and federal public health and legal mandates are in place to govern the collection and use of these data. Despite the prima facie appeal of "opt-in" and simila...

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عنوان ژورنال:
  • Birth defects research. Part A, Clinical and molecular teratology

دوره 97 11  شماره 

صفحات  -

تاریخ انتشار 2013