46,XX/46XY chromosome complement in amniotic fluid cell culture followed by the birth of a normal female child

Prenat Diagn. 1982 Apr;2(2):127-31. doi: 10.1002/pd.1970020209.


Experience indicates that the most likely explanation for a mixture of 46,XX/46,XY cells in an amniotic fluid sample is that of maternal cell contamination and that a normal male child is to be expected at birth. We report the bith of a normal female child following prenatal diagnosis of such a mixture. Extensive postnatal studies failed to reveal an XY cell line. The possible sources of the XY cell line are discussed, as are the various techniques that were applied in an effort to discover it's origin. Cross-contamination of samples could be ruled out and there was no evidence of an unsuspected twin pregnancy. It is clear from this case that not all 46,XX/46,XY results obtained in amniotic fluid can be assumed to represent maternal cell contamination and some effort should be made to eliminate other potential sources for such a mixture.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Amniocentesis
  • Amniotic Fluid / cytology*
  • Female
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Pregnancy
  • Prenatal Diagnosis*
  • Sex Chromosome Aberrations / diagnosis*