Yakut S, Cetin Z, Sanhal C, Karaman B, Mendilcioglu I, Karauzum S B
Genet Couns. 2015;26(2):243-7.
We here report a prenatal case with de novo pericentric inversion inv(2)(p11.2q13). A 20-years-old G1PO woman was referred for amniocentesis at 17 weeks of gestation, because of a positive second trimester screening test for aneuploidy. A de novo pericentric inversion inv(2)(p11.2q13) was detected during conventional cytogenetic analysis. Array-CGH analysis of the fetus showed no subtle chromosomal imbalances at the breakpoints. Genetic counseling was given to the family and the family decided to continue the pregnancy. To our knowledge, our case is the third prenatally detected de novo case with inv(2)(p11.2q13), and also the first case in which molecular karyotyping analysis were also applied.
我们在此报告一例新发的2号染色体臂间倒位inv(2)(p11.2q13)的产前病例。一名20岁、孕1产0的女性因孕中期非整倍体筛查试验呈阳性,于妊娠17周时转诊接受羊水穿刺检查。在常规细胞遗传学分析中检测到新发的2号染色体臂间倒位inv(2)(p11.2q13)。对胎儿进行的阵列比较基因组杂交分析显示,断点处无细微的染色体失衡。已为该家庭提供遗传咨询,该家庭决定继续妊娠。据我们所知,我们的病例是第三例产前检测到的新发inv(2)(p11.2q13)病例,也是第一例应用分子核型分析的病例。