The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome

Prenat Diagn. 2017 Jan;37(1):53-60. doi: 10.1002/pd.4864. Epub 2016 Jul 25.

Abstract

Cell-free DNA testing is increasingly being used to screen pregnant women for fetal aneuploidy. This technology may also identify microdeletion syndromes, including 22q11.2 deletion syndrome, the most common microdeletion syndrome, and the 22q11.2 duplication syndrome. The purpose of this paper is to provide an overview of the 22q11.2 deletion syndrome, to review the early experience with cell-free DNA screening for this deletion and to consider the potential benefits that may be associated with prenatal detection of the deletion. © 2016 John Wiley & Sons, Ltd.

MeSH terms

  • DiGeorge Syndrome / diagnosis*
  • DiGeorge Syndrome / genetics
  • Female
  • Humans
  • Pregnancy
  • Prenatal Diagnosis*