Endocrine profiles and cycle characteristics of infertile 17α-hydroxylase/17,20-lyase Deficiency Patients undergoing assisted Reproduction Treatment: a retrospective cohort study

• Ngā kaituhi matua: Ping Pan (Author), Lingyan Zheng (Author), Jia Huang (Author), Xiaoli Chen (Author), Renmin Ni (Author), Qingxue Zhang (Author), Dongzi Yang (Author), Yu Li (Author)
• Hōputu: Pukapuka
• I whakaputaina: BMC, 2023-06-01T00:00:00Z.
• Ngā marau: article
• Urunga tuihono: Connect to this object online.

Abstract Background 17α-hydroxylase/17,20-lyase deficiency (17-OHD) is a rare form of congenital adrenal hyperplasia caused by CYP17A1 gene variants. Female patients with 17-OHD demonstrate a broad clinical spectrum, including oligomenorrhea or amenorrhea and infertility, often as the sole manifesta...