Brothman A R, Newlin A, Phillips S E, Kinzie G Q, Leichtman L G
Department of Pediatrics, Eastern Virginia Medical School, Norfolk.
Clin Genet. 1993 Sep;44(3):139-41. doi: 10.1111/j.1399-0004.1993.tb03864.x.
An unusual case of an X chromosome with a pericentric inversion (p11.3q21.3) was detected prenatally in a male fetus. This inversion has not been previously characterized. Although the inverted chromosome was transmitted through the mother, no living males on the maternal side were detected with the aberrant chromosome. Replication studies were performed on cultures of maternal peripheral blood lymphocytes, and it was determined that the inverted X chromosome was early replicating in approximately half of the cells. Following genetic counseling, the pregnancy was continued and a healthy male infant was delivered at term. Cytogenetic analysis of peripheral blood performed in the newborn period confirmed the prenatal findings. The child is developing normally at 3 years of age.
在一名男性胎儿中产前检测到一例异常的X染色体,其发生了臂间倒位(p11.3q21.3)。这种倒位此前尚未有特征描述。尽管这条倒位染色体是通过母亲遗传的,但在母系中未检测到携带异常染色体的存活男性。对母亲外周血淋巴细胞培养物进行了复制研究,确定这条倒位的X染色体在大约一半的细胞中是早期复制的。经过遗传咨询后,妊娠继续进行,足月时分娩出一名健康男婴。新生儿期对外周血进行的细胞遗传学分析证实了产前检查结果。这孩子3岁时发育正常。