Six prenatally diagnosed cases of trisomy 9 are reported and 22 previo
usly reported cases are reviewed; the difficulty of genetic counsellin
g for such cases and the variation in the percentage of trisomic cells
in different tissues, thus making accurate diagnosis of trisomy 9 dif
ficult, are emphasized. In addition to karyotyping results, ultrasound
findings are important in achieving diagnoses. Finally, a course of a
ction when prenatal trisomy 9 is detected is proposed.