Schuring-Blom G H
Academisch Medisch Centrum/Universiteit van Amsterdam, afd. Klinische Genetica, Meibergdreef 15, 1105 AZ Amsterdam.
Ned Tijdschr Geneeskd. 2002 Dec 21;146(51):2470-4.
Chromosomal mosaicism is when two (or more) cell lines with different chromosomal complements are found within one individual. Mosaicism can be found in all tissues but may also be confined to a specific tissue. During pregnancy the aberrant cell line, often with a trisomy, may be confined to the placenta. In prenatal diagnosis, more specifically in chorionic villus sampling, this can interfere with the results and may necessitate follow-up investigation with amniotic fluid cell culture. Confined placental mosaicism can have no visible effect whatsoever on foetal development, but can also lead to serious foetal problems, depending on the chromosome involved. Uniparental disomy in the diploid cell line of the mosaicism may also have a negative effect on the foetal phenotype. In the case of the reverse situation, where the normal diploid cell line is confined to the placenta and the foetus has trisomy 13 or 18, it has been suggested that the diploid cell line might play a role in intrauterine survival; a recent study by the present authors could not confirm this view.
染色体嵌合体是指在一个个体内发现两种(或更多)具有不同染色体组成的细胞系。嵌合体可在所有组织中出现,但也可能局限于特定组织。在孕期,异常细胞系(通常为三体)可能局限于胎盘。在产前诊断中,更具体地说是在绒毛取样时,这可能会干扰结果,可能需要通过羊水细胞培养进行后续调查。局限性胎盘嵌合体可能对胎儿发育没有任何可见影响,但也可能导致严重的胎儿问题,这取决于所涉及的染色体。嵌合体二倍体细胞系中的单亲二体也可能对胎儿表型产生负面影响。在相反的情况下,即正常二倍体细胞系局限于胎盘而胎儿患有13或18三体,有人提出二倍体细胞系可能在子宫内存活中起作用;本文作者最近的一项研究未能证实这一观点。