Chorionic villus sampling after first trimester diagnosis of fetal cystic hygroma colli

Eur J Obstet Gynecol Reprod Biol. 1989 Nov;33(2):141-6. doi: 10.1016/0028-2243(89)90206-2.

Abstract

Diagnostic findings of four cases of cystic hygroma discovered at 11 weeks of gestation are reported. The discovery of cystic hygroma by echotomography was followed by sample taking of chorionic villi which revealed one case of monosomy X and three cases of trisomy 18. Caryotype determination in the presence of cystic hydroma is essential for diagnostic confirmation and subsequent genetic counselling.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chorionic Villi Sampling
  • Chromosome Aberrations
  • Chromosomes, Human, Pair 18
  • Female
  • Gestational Age
  • Humans
  • Lymphatic System / abnormalities*
  • Lymphocele / diagnosis
  • Lymphocele / embryology
  • Lymphocele / genetics
  • Male
  • Pregnancy
  • Prenatal Diagnosis*
  • Trisomy
  • Turner Syndrome / diagnosis
  • Turner Syndrome / genetics
  • Ultrasonography