Prenatal genetic diagnosis of Down's syndrome

Expert Rev Mol Diagn. 2002 Nov;2(6):605-15. doi: 10.1586/14737159.2.6.605.

Abstract

Down's syndrome is a common cause of birth defects and mental retardation. Prenatal screening and diagnosis of Down's syndrome is important to any pregnant woman interested in the health of her fetus and is of particular concern to the growing number of advanced maternal age women who are at increased risk of an affected pregnancy. Prenatal screening tests, performed in the first and second trimester, are based on maternal age, serum tests and fetal ultrasound. Definitive diagnosis requires amniocentesis or chorionic villus sampling. Hopefully, these invasive tests can, one day, be replaced with safer methods of obtaining fetal cells. Molecular genetic techniques are augmenting traditional chromosome analysis, broadening the range of identifiable genetic disorders and allowing earlier results.

Publication types

  • Review

MeSH terms

  • Amniocentesis
  • Biomarkers
  • Chorionic Villi Sampling
  • Chromosomes, Human, Pair 21
  • Down Syndrome / diagnosis*
  • Down Syndrome / diagnostic imaging
  • Down Syndrome / embryology
  • Down Syndrome / genetics
  • Female
  • Fetal Diseases / diagnosis*
  • Fetal Diseases / diagnostic imaging
  • Fetal Diseases / genetics
  • Genetic Testing
  • Humans
  • In Situ Hybridization, Fluorescence
  • Maternal Age
  • Molecular Diagnostic Techniques*
  • Nucleic Acid Hybridization
  • Pregnancy
  • Pregnancy Trimesters
  • Preimplantation Diagnosis / methods
  • Prenatal Diagnosis / methods*
  • Trisomy
  • Ultrasonography, Prenatal*
  • alpha-Fetoproteins / analysis

Substances

  • Biomarkers
  • alpha-Fetoproteins