Upadhyay Divyesh, Al Halaby Rajia, Anandt Sudha, Albuz Firas, Varghese Merlin Mary, Peramo Braulio
Clinical Department, Al Ain Fertility Center, Al Ain, Abu Dhabi, United Arab Emirates.
Genetics Department, Al Ain Fertility Center, Al Ain, Abu Dhabi, United Arab Emirates.
F S Rep. 2024 Nov 7;5(4):439-452. doi: 10.1016/j.xfre.2024.10.006. eCollection 2024 Dec.
To present a case of a couple with 20 years of infertility and 10 recurrent in vitro fertilization (IVF) failures, identifying a paternal complex chromosome rearrangement using high-resolution karyotype together with preimplantation genetic testing for structural rearrangements (PGT-SR) and utilizing IVF-intracytoplasmic sperm injection to achieve a successful pregnancy.
Case report.
Al Ain Fertility Center, Abu Dhabi, United Arab Emirates.
A 40-year-old male patient and a 37-year-old female patient with a history of infertility and recurrent IVF failures.
In vitro fertilization-intracytoplasmic sperm injection with high-resolution karyotype and PGT-SR.
Identification of chromosomal abnormalities, successful embryo development, pregnancy outcome, and newborn karyotyping.
Karyotyping revealed a paternal complex chromosome rearrangement, t(3;4;12) (q21;q33;q21), and a chromosomal polymorphism in the female (1qh+). In vitro fertilization-intracytoplasmic sperm injection with PGT-SR produced one euploid/balanced female embryo from 20 embryos across 8 cycles. The patient conceived after hormone replacement therapy and frozen embryo transfer, resulting in an uneventful, full-term pregnancy and delivery of a healthy baby via C-section. Newborn karyotyping was normal (46,XX).
High-resolution karyotype and PGT-SR should be offered to patients undergoing IVF, especially those with severe male factors, recurrent IVF failures, implantation failures, or recurrent pregnancy losses, to enhance the chances of a successful pregnancy.
介绍一对有20年不孕史且体外受精(IVF)失败10次的夫妇的病例,通过高分辨率核型分析以及植入前结构重排基因检测(PGT-SR)识别父系复杂染色体重排,并利用IVF-卵胞浆内单精子注射术成功妊娠。
病例报告。
阿拉伯联合酋长国阿布扎比艾因生育中心。
一名40岁男性患者和一名37岁女性患者,有不孕和反复IVF失败史。
进行高分辨率核型分析和PGT-SR的IVF-卵胞浆内单精子注射术。
染色体异常的识别、胚胎的成功发育、妊娠结局及新生儿核型分析。
核型分析显示父系存在复杂染色体重排,即t(3;4;12) (q21;q33;q21),女性存在染色体多态性(1qh+)。采用PGT-SR的IVF-卵胞浆内单精子注射术在8个周期的20个胚胎中产生了1个整倍体/平衡的女性胚胎。患者在激素替代疗法和冷冻胚胎移植后受孕,妊娠过程顺利,足月分娩,通过剖宫产产下一名健康婴儿。新生儿核型分析正常(46,XX)。
对于接受IVF治疗的患者,尤其是那些存在严重男性因素、反复IVF失败、着床失败或反复妊娠丢失的患者,应提供高分辨率核型分析和PGT-SR,以提高成功妊娠的几率。