Hayata I, Oshimura M, Marinello M J, Bannerman R M, Sandberg A A
J Med Genet. 1976 Aug;13(4):320-3. doi: 10.1136/jmg.13.4.320.
Because of multiple abnormalities in her children, a young mother was investigated and shown to have a 47,XXX chromosome constitution. Additional C group chromosomes without visible centromeric constrictions were found in a number of cells from the peripheral blood, and using C and Q banding techniques these chromosomes were identified as X chromosomes. Analysis of the banding karyotypes of 300 cells revealed that the acentric X chromosomes had the ability to replicate and that this replication was associated with non-disjunction leading to aneuploid cells. Even though cultured skin cells did not have acentric or extra chromosomes in addition to the triple-X, examination of buccal mucosa cells for the presence of X-bodies suggested that the phenomenon of non-disjunction was present in the epithelial cells of the patient. In addition to the X without a visible centromeric constriction, either acentric D or E chromosomes were found. The data suggest that a functional defect in the cells per se is responsible for the appearance of the acentric chromosomes.
由于她的孩子存在多种异常情况,对一位年轻母亲进行了检查,结果显示其染色体组成为47,XXX。在外周血的许多细胞中发现了额外的无可见着丝粒缢痕的C组染色体,运用C带和Q带技术,这些染色体被鉴定为X染色体。对300个细胞的带型核型分析表明,无着丝粒X染色体具有复制能力,且这种复制与导致非整倍体细胞的不分离现象有关。尽管培养的皮肤细胞除了三体X外没有无着丝粒或额外的染色体,但对颊黏膜细胞中X小体的检测表明,患者上皮细胞中存在不分离现象。除了无可见着丝粒缢痕的X染色体外,还发现了无着丝粒的D或E染色体。数据表明,细胞本身的功能缺陷是无着丝粒染色体出现的原因。