Cystic hygroma: prenatal diagnosis and genetic counselling

Prenat Diagn. 1985 May-Jun;5(3):221-7. doi: 10.1002/pd.1970050310.

Abstract

Six cases of cystic hygromas detected during second trimester ultrasound examination are reported: 4 fetuses (67 per cent) had a 45, X karyotype, 1 fetus had trisomy 18, 1 fetus had a normal karyotype (46,XX) and at autopsy multiple anomalies were observed. In the latter case the family history suggested an autosomal recessive pattern of inheritance. In order to reach a definite diagnosis and give proper genetic counselling when a fetus is found to have cystic hygroma, a fetal karyotype as well as a family and reproductive history should be obtained.

Publication types

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

MeSH terms

  • Adult
  • Female
  • Fetus / pathology
  • Genetic Counseling*
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Lymphangioma / diagnosis*
  • Lymphangioma / genetics
  • Lymphangioma / pathology
  • Male
  • Pregnancy
  • Pregnancy, Multiple
  • Prenatal Diagnosis*
  • Twins
  • Ultrasonography*