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

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...

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主要な著者:	Ping Pan, Lingyan Zheng, Jia Huang, Xiaoli Chen, Renmin Ni, Qingxue Zhang, Dongzi Yang, Yu Li
フォーマット:	Artigo
言語:	Inglês
出版事項:	BMC 2023-06-01
シリーズ:	Journal of Ovarian Research
主題:	17α-hydroxylase/17,20-lyase deficiency Congenital adrenal hyperplasia Infertility Pregnancy Assisted reproductive technique
オンライン･アクセス:	https://doi.org/10.1186/s13048-023-01190-6
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