Cystic hygroma and hydrops fetalis in a fetus with trisomy 13

Clin Genet. 1983 Nov;24(5):389-91. doi: 10.1111/j.1399-0004.1983.tb00091.x.

Abstract

We report a case of trisomy 13 with cystic hygroma and generalized hydrops fetalis diagnosed prenatally by routine ultrasound prior to genetic amniocentesis in a 34-year-old woman. Although fetal cystic hygroma is usually associated with a 45,X karyotype, this and other previous reports suggest that it may be seen in association with other chromosomal and nonchromosomal abnormalities as well. Thus, a diagnosis of Turner Syndrome should not be made on the basis of a cystic hygroma observed by prenatal sonography alone.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chromosomes, Human, 13-15*
  • Edema / genetics*
  • Female
  • Fetal Diseases / genetics*
  • Humans
  • Lymphangioma / genetics*
  • Male
  • Pregnancy
  • Prenatal Diagnosis
  • Trisomy*
  • Ultrasonography