Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin

Prenat Diagn. 2003 Jul;23(7):572-4. doi: 10.1002/pd.645.

Abstract

Prenatal diagnosis of 5p deletion syndrome, or cri du chat, following an abnormally low measurement of a screening of serum human chorionic gonadotrophin (hCG), is reported. Karyotyping following amniocentesis revealed a terminal deletion in the short arm of one chromosome 5. The pregnancy was electively terminated. 5p deletion syndrome has been described with abnormally high hCG levels and normal hCG levels. This is the first report of its association with abnormally low levels. The association between chromosomal abnormalities and hCG is discussed.

Publication types

  • Case Reports

MeSH terms

  • Abortion, Induced
  • Adult
  • Amniocentesis
  • Chorionic Gonadotropin, beta Subunit, Human / blood*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 5*
  • Cri-du-Chat Syndrome / blood
  • Cri-du-Chat Syndrome / diagnosis*
  • Cri-du-Chat Syndrome / genetics
  • Diagnosis, Differential
  • Female
  • Fetal Diseases / blood
  • Fetal Diseases / diagnosis*
  • Fetal Diseases / genetics
  • Humans
  • Karyotyping
  • Pregnancy
  • Prenatal Diagnosis*

Substances

  • Chorionic Gonadotropin, beta Subunit, Human