Androgen insensitivity syndrome after preimplantation genetic diagnosis for sex selection: A case report

被引：3
|
作者：
Kilani, Zaid [1 ]
Dajani, Yahia [1 ]
Qaddomi, Eva [1 ]
Hassan, Lamia Haj [1 ]
机构：
[1] Farah Hosp, Amman, Jordan
来源：
FERTILITY AND STERILITY | 2009年 / 92卷 / 03期
关键词：
Sex selection; preimplantation genetic diagnosis; gender; androgen insensitivity;
D O I：
10.1016/j.fertnstert.2009.05.046
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
Objective: To report the first case of androgen insensitivity syndrome after preimplantation genetic diagnosis (PGD) for sex selection. Design: Case report. Setting: The Farah Hospital (a private tertiary referral fertility center). Patient(s): A healthy woman with three daughters underwent PGD for sex selection, seeking a male baby. Intervention(s): PGD was done and the woman became pregnant. Ultrasound examination showed female phenotype. Amniocentesis was performed and culture of cells confirmed XY karyotype. Result(s): Karyotyping confirmed the diagnosis of XY genotype and pregnancy was terminated. Conclusion(s): Although androgen insensitivity syndrome is very rare, it can occur in cases of PGD for sex selection. (Fertil Steril (R) 2009;92:1169.e5-e7. (C)2009 by American Society for Reproductive Medicine.)
引用
收藏
页码：1169.e5 / 1169.e7
页数：3
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