Courtens W, Petersen M B, Noël J C, Flament-Durand J, Van Regemorter N, Delneste D, Cochaux P, Verschraegen-Spae M R, Van Roy N, Speleman F
Laboratory of Cytogenetics, Brugmann University Hospital, Brussels, Belgium.
Am J Med Genet. 1994 Jul 1;51(3):260-5. doi: 10.1002/ajmg.1320510318.
Foetal blood sampling was performed at 35 weeks of gestation due to abnormal foetal ultrasound findings. There was apparent monosomy 21 (45,XX,-21) in all mitoses analyzed. The infant died at 37 weeks during delivery. Examination disclosed facial anomalies, clubfeet, hypoplasia of the left urogenital tract, agenesis of corpus callosum, ventricular dilatation, and heterotopias. Reevaluation of the karyotype showed an unbalanced translocation t(1;21) (q44;q22.11) which resulted from a maternal balanced translocation. These findings were confirmed by fluorescence in situ hybridization and molecular studies with chromosome 21 specific markers. The latter showed a proximal deletion of the maternally derived chromosome 21 including all loci from centromere down to the D21S210 locus. This case illustrates the need for complementary cytogenetic and molecular investigations in cases of apparent monosomy 21.
由于胎儿超声检查结果异常,在妊娠35周时进行了胎儿血样采集。在所有分析的有丝分裂中均明显存在21号染色体单体(45,XX,-21)。婴儿在37周分娩时死亡。检查发现有面部畸形、马蹄内翻足、左泌尿生殖道发育不全、胼胝体发育不全、脑室扩张和异位。对核型的重新评估显示存在不平衡易位t(1;21) (q44;q22.11),这是由母亲的平衡易位导致的。这些发现通过荧光原位杂交和使用21号染色体特异性标记的分子研究得到证实。后者显示母源21号染色体近端缺失,包括从着丝粒到D21S210位点的所有基因座。该病例说明了在明显的21号染色体单体病例中进行补充细胞遗传学和分子研究的必要性。