Idiopathic hypogonadotropic hypogonadism caused by compound heterozygosity for two novel mutations in the GNRH1 gene: a case report

Idiopathic hypogonadotropic hypogonadism (IHH) is a rare congenital or acquired genetic disorder caused by gonadotropin-releasing hormone (GnRH) deficiency. IHH patients are divided into two major groups, hypo...

Source: BMC Endocrine Disorders - October 5, 2023 Category: Endocrinology Authors: Qingqing Tian, Jingjing Tang, Lihong Wang, Jiaojiao Liu, Xiangshan Li, Zhuozhuo Cao and Zhufang Tian Tags: Case report Source Type: research