Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 Oct;35(10):931-5.
doi: 10.1002/pd.4647. Epub 2015 Jul 27.

Changing trends in carrier screening for genetic disease in the United States

Affiliations
Review

Changing trends in carrier screening for genetic disease in the United States

Shivani B Nazareth et al. Prenat Diagn. 2015 Oct.

Abstract

Genetic disease is the leading cause of infant death in the United States, accounting for approximately 20% of annual infant mortality. Advances in genomic medicine and technological platforms have made possible low cost, pan-ethnic expanded genetic screening that enables obstetric care providers to offer screening for over 100 recessive genetic diseases. However, the rapid integration of genomic medicine into routine obstetric practice has raised some concerns about the practical implementation of such testing. These changing trends in carrier screening, along with concerns and potential solutions, will be addressed.

PubMed Disclaimer

References

    1. Collins FS. The Language of Life: DNA and the Revolution in Personalized Medicine. (1st edn), New York: Harper, 2010;23–58.
    1. Kaback MM. Population‐based genetic screening for reproductive counseling: the Tay–Sachs disease model. Eur J Pediatr 2000;159(Suppl 3):S192–5. - PubMed
    1. American College of Obstetricians and Gynecologists Committee on Genetics . ACOG Committee Opinion No. 486: update on carrier screening for cystic fibrosis. Obstet Gynecol 2011;117(4):1028–31. - PubMed
    1. Watson MS, Cutting GR, Desnick RJ, et al. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. Genet Med 2004;6(5):387–91. - PMC - PubMed
    1. Gross SJ, Pletcher BA, Monaghan KG, et al. Carrier screening in individuals of Ashkenazi Jewish descent. Genet Med 2008;10(1):54–6. - PMC - PubMed