First trimester diagnosis and screening for fetal aneuploidy

Genet Med. 2008 Jan;10(1):73-5. doi: 10.1097/GIM.0b013e31815efde8.

Abstract

Maternal serum screening for neural tube defects and fetal aneuploidy in the second trimester has been incorporated into obstetrical practice over the past two decades. Now, as a result of several multicenter trials, first trimester screening between 11 and 14 weeks has been shown to be an effective and reliable screening test for Down syndrome and trisomy 18. Benefits of first trimester screening include earlier identification of the pregnancy at risk for fetal aneuploidy and anatomic defects, in particular, cardiac anomalies, and the option of earlier diagnosis by chorionic villus sampling, if available. This policy updates the American College of Medical Genetics policy statement entitled Second Trimester Maternal Serum Screening for Fetal Open Neural Tube Defects and Aneuploidy (2004) and complements the sections of American College of Medical Genetic's Standards and Guidelines for Clinical Genetics Laboratories entitled "Prenatal screening for Down syndrome that includes first trimester biochemistry and/or ultrasound measurements."

Publication types

  • Practice Guideline

MeSH terms

  • Aneuploidy*
  • Down Syndrome / diagnosis
  • Down Syndrome / genetics
  • Female
  • Fetus*
  • Genetic Markers
  • Genetic Testing / standards*
  • Genetic Testing / trends
  • Humans
  • Nuchal Translucency Measurement / standards
  • Nuchal Translucency Measurement / trends
  • Pregnancy
  • Pregnancy Trimester, First / genetics*
  • Prenatal Diagnosis / standards*
  • Prenatal Diagnosis / trends
  • Societies, Medical
  • United States

Substances

  • Genetic Markers