Mosaicism of 46,XX/47,XX,+9/47,XX,+?mar in the same amniotic fluid with apparent loss of one cell line after delivery

Prenat Diagn. 1989 May;9(5):373-5. doi: 10.1002/pd.1970090513.

Abstract

A 46,XX;47,XX,+9;47,XX,+?mar karyotype was detected in an amniotic fluid cell culture and confirmed in a subsequent fetal blood sample from a 40-year-old woman. After termination of the pregnancy, none of the 186 mitoses obtained from a second blood sample was trisomic for chromosome 9 (p less than 0.001). Selection against cells containing trisomy 9 is postulated to explain the disappearance of the lymphocyte clone.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Amniotic Fluid / cytology*
  • Cells, Cultured
  • Chromosomes, Human, Pair 9*
  • Female
  • Fetal Blood / cytology
  • Humans
  • Karyotyping
  • Mosaicism*
  • Pregnancy
  • Prenatal Diagnosis*
  • Trisomy*