Nisani R, Chemke J, Voss R, Appelman Z, Caspi B, Lewin A, Dar H, Reiter A
Clinical Genetics Unit, Kaplan Hospital, Rehovot, Israel.
Prenat Diagn. 1989 Apr;9(4):223-6. doi: 10.1002/pd.1970090402.
Chromosomal mosaicism is one of several unanswered dilemmas in first-trimester prenatal diagnosis. We report the course of a pregnancy in which a normal karyotype was detected on direct CVS preparation and fetal blood, 100 per cent trisomy 21 in one long-term CVS culture, and low-rate trisomy 21 mosaicism in a second long-term CVS culture and amniocentesis. The phenotypically normal infant had a 6 per cent mosaicism of trisomy 21. It appears that a persistent low-rate mosaicism in different tissues may be indicative of the true status of the fetus.