Successful live birth after intracytoplasmic sperm injection using testicular sperm in non-mosaic Klinefelter syndrome  

作　　者：Sonia Jellad Ramzi Arfaoui Nesrine Souayah Fatma Hammami 

机构地区：[1]Department of Sterility Exploration and Assisted Medical Procreation,Military Hospital of Tunis,1008,Montfleury Tunis,Tunisia [2]Faculty of Medecine of Tunis,University of Tunis El Manar,Tunisia [3]Department of Gynecology,Military Hospital of Tunis,Tunisia

出　　处：《Asian pacific Journal of Reproduction》2022年第1期51-52,共2页亚太生殖杂志（英文版）

摘　　要：Klinefelter syndrome represents one of the most common male sex chromosome disorders with a prevalence of 1 out of 500 male newborns[1].The syndrome is marked by the presence of an additional X chromosome in human males.It manifests mostly as 47,XXY,and can take the mosaic form as 46,XY/47,XXY.A 36-year-old adult had been referred to our department for primary infertility exploration.Prior semen analyses had demonstrated azoospermia.The patient had no particular pathological history.The physical examination revealed a well-masculinized body with normal hair density and distribution,without gynecomastia.However,genital examination revealed bilateral hypotrophic testes.

关 键 词：INJECTION KLINEFELTER mostly 

分 类 号：R59[医药卫生—内科学]