Varela M, Wang N, Cerrillo M
Hum Genet. 1987 Jan;75(1):93-4. doi: 10.1007/BF00273851.
A 46,XX,inv(12)pat/47,XX,i(Xq),inv(12)pat was diagnosed prenatally in a 36-year-old woman whose husband was a known carrier of a pericentric inversion of chromosome 12. The diagnosis was confirmed in fetal tissue. Terminal bromodeoxyuridine (BrdU) labelling demonstrated that in the line with 46 chromosomes one X was late replicating, while one X and the i(Xq) were late replicating in 100% of the cells with 47 chromosomes. We present the first case of this type of sex chromosome mosaicism. Genetic counseling presented difficulties since it was not possible to predict the fetal phenotype.
一名36岁女性产前被诊断为46,XX,inv(12)pat/47,XX,i(Xq),inv(12)pat,其丈夫是已知的12号染色体臂间倒位携带者。该诊断在胎儿组织中得到证实。末端溴脱氧尿苷(BrdU)标记显示,在具有46条染色体的细胞系中,一条X染色体复制延迟,而在具有47条染色体的所有细胞中,一条X染色体和i(Xq)均复制延迟。我们报告了首例这种类型的性染色体嵌合体病例。由于无法预测胎儿表型,遗传咨询面临困难。