Azargoon Azam, Azad Nahid
Abnormal Uterine Bleeding Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Department of Infertility, Amir-AL-Momenin Hospital, Semnan University of Medical Sciences, Semnan, Iran.
J Reprod Infertil. 2020 Oct-Dec;21(4):308-311. doi: 10.18502/jri.v21i4.4325.
Infertility is a problem affecting a large number of couples in the world. One of the causes of infertility can be chromosomal rearrangements such as insertions. In this case report study, the outcome of two intra-cytoplasmic sperm injection (ICSI) cycles of an infertile woman with de novo chromosomal insertion is explained.
A couple with a 10-year history of infertility referred to our infertility clinic. The husband had a daughter in his first previous marriage. The wife had a 7 and a 10 year history of infertility in the first and second marriages, respectively. In the first marriage, she reported a history of 2 failed intra-uterine insemination (IUI) cycles. In the second marriage, she had a history of 1 spontaneous abortion at 12 weeks of pregnancy, 4 failed IUI cycles, and 1 failed ICSI cycle. The couple was subjected to ICSI cycles twice and failed due to embryo development arrest. The couple referred for karyotyping. The husband showed a normal male karyotype. In comparison, the wife revealed an abnormal female karyotype with two rearrangements: chromosome 13 with an interstitial deletion between bands q14.2 and q21.1, and a derivative chromosome 7 containing this segment of chromosome 7 as an insertion onto short arm at the p14 position.
To the best of our knowledge, this is the first report of insertion 46 XX, ins(7:13)(p14; q14.2q21.1) which is associated with the embryo development arrest following assisted reproductive technique.
不孕是一个影响全球大量夫妇的问题。不孕的原因之一可能是染色体重排,如插入。在本病例报告研究中,解释了一名患有新发染色体插入的不孕女性两个胞浆内单精子注射(ICSI)周期的结果。
一对有10年不孕史的夫妇前来我们的不孕诊所就诊。丈夫在前一段婚姻中有一个女儿。妻子在第一段和第二段婚姻中分别有7年和10年的不孕史。在第一段婚姻中,她报告有2次宫内人工授精(IUI)周期失败的病史。在第二段婚姻中,她有一次妊娠12周时自然流产的病史、4次IUI周期失败以及1次ICSI周期失败。这对夫妇接受了两次ICSI周期治疗,但由于胚胎发育停滞而失败。这对夫妇前来进行核型分析。丈夫显示正常男性核型。相比之下,妻子显示异常女性核型,有两种重排:13号染色体在q14.2和q21.1带之间有间质缺失,以及一条衍生的7号染色体,该染色体包含7号染色体的这一片段,插入到短臂的p14位置。
据我们所知,这是46 XX,ins(7:13)(p14; q14.2q21.1)插入的首次报告,该插入与辅助生殖技术后胚胎发育停滞有关。