Qumsiyeh M B, Tomasi A, Taslimi M
Cytogenetics Laboratory, Duke University Medical Center, Durham, NC 27710, USA.
J Med Genet. 1995 Dec;32(12):991-3. doi: 10.1136/jmg.32.12.991.
A patient was referred for amniocentesis because of advanced maternal age and polyhydramnios. The fetal karyotype was a mosaic 46,XX,del(18)(p11.1)/46,XX,-18,+i(18q)de novo. The deletion appeared to encompass the whole short arm as evidenced by G banding and in situ hybridisation. However, telomere sequences were found on both ends of the deleted chromosome as well as the isochromosome. The normal 18 and the isochromosome showed more alphoid sequences than the del(18). Subsequent passages of the cell lines showed an increase in the frequency of the isochromosome from 20% to about 30%. Possible mechanisms are discussed.
一名患者因母亲年龄较大及羊水过多而接受羊膜穿刺术。胎儿核型为嵌合型46,XX,del(18)(p11.1)/46,XX,-18,+i(18q),为新发突变。G显带和原位杂交显示,该缺失似乎涵盖了整个短臂。然而,在缺失染色体以及等臂染色体的两端均发现了端粒序列。正常的18号染色体和等臂染色体显示出比del(18)更多的α卫星序列。细胞系的后续传代显示等臂染色体的频率从20%增加到约30%。文中讨论了可能的机制。