Chromosomal abnormalities associated with a single umbilical artery

Prenat Diagn. 1992 Nov;12(11):965-8. doi: 10.1002/pd.1970121118.

Abstract

A single umbilical artery was seen in 10 out of 117 cytogenetically abnormal pregnancies. The abnormal karyotypes found to be associated with a single umbilical artery were trisomy 18 (n = 5), monosomy X (n = 2), triploidy (n = 1), sex chromosome (47,XYY; n = 1) and translocation (46t(X,5)(q13p15);n = 1). With the exception of the translocation case, all cases with a single umbilical artery had anatomical defects which were detectable ultrasonographically. This suggests that a single umbilical artery alone is not an indication for prenatal fetal karyotyping.

MeSH terms

  • Chromosome Aberrations / diagnostic imaging*
  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 18
  • Chromosomes, Human, Pair 5
  • Female
  • Humans
  • Pregnancy
  • Trisomy
  • Ultrasonography
  • Umbilical Arteries / abnormalities*
  • X Chromosome
  • Y Chromosome