DuPont B R, Huff R W, Ridgway L E, Stratton R F, Moore C M
Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio 78284-7762.
Am J Med Genet. 1994 Mar 1;50(1):21-7. doi: 10.1002/ajmg.1320500105.
We report the use of fluorescent in situ hybridization (FISH) with a DNA library of chromosome 1-specific probes to confirm the karyotype, 46,XY,15+der15,t(1;15)(q32.1; q26.3), obtained by prenatal periumbilical blood sampling from a fetus who exhibited multiple abnormalities by ultrasound examination. GTG-banding of chromosomes obtained from the mother showed a normal karyotype, while the father was unavailable for study. The propositus was born at 37 weeks gestation and survived for several weeks. Cytogenetic analysis performed after the birth of the male infant with multiple anomalies verified partial trisomy 1q. This patient is compared with other partial trisomy 1q patients reported in the literature. The usefulness of FISH is demonstrated in situations where fetal abnormalities are present with de novo chromosomal rearrangements where paternal chromosomes are unavailable for study.
我们报告了使用荧光原位杂交(FISH)技术,结合1号染色体特异性探针的DNA文库来确认核型,即46,XY,15+der15,t(1;15)(q32.1; q26.3),该核型是通过对一名经超声检查显示有多种异常的胎儿进行产前脐周血采样获得的。从母亲身上获取的染色体进行GTG显带显示核型正常,而父亲无法进行研究。先证者在妊娠37周时出生,并存活了几周。对患有多种异常的男婴出生后进行的细胞遗传学分析证实了1q部分三体。将该患者与文献中报道的其他1q部分三体患者进行了比较。在胎儿存在异常且有新发染色体重排而无法对父源染色体进行研究的情况下,证明了FISH的实用性。