EUROPEAN COLLABORATIVE STUDY ON PRENATAL-DIAGNOSIS - MOSAICISM, PSEUDOMOSAICISM AND SINGLE ABNORMAL-CELLS IN AMNIOTIC-FLUID CELL-CULTURES

被引:115
作者
BUI, TH
ISELIUS, L
LINDSTEN, J
机构
关键词
D O I
10.1002/pd.1970040710
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A report is given of the results of a European collaborative study on mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures. The mean frequency of cases with mosaicism was 0.10%, with pseudomosaicism 0.64% and with single abnormal cells 2.83% in a series of 44,170 amniotic fluid samples. There was no significant difference between the colony (in situ) and the flask method with regard to the frequency of mosaicism. Pseudomosaicism and single abnormal cells were more frequent in cases studied with the flask method probably due to other factors than the method of cultivation of the cells. The frequency of maternal cell contamination was 0.17% and the frequency of wrong sex assignment was 0.11%. A more correct estimation is obtained if these frequencies are doubled. There was a considerable variation between laboratories with regard to the frequencies given above. One reason for this variation is that there are no sharp limits between mosaicism, pseudomosaicism and single abnormal cells. Thus the material contained cases diagnosed as having pseudomosaicism which turned out to be mosaics at birth and to have an abnormal phenotype. These cases were very rare but pose a definite problem in prenatal cytogenetic diagnosis.
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页码:145 / 162
页数:18
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