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...

ver descrição completa

Detalhes bibliográficos

Principais autores:	Ping Pan, Lingyan Zheng, Jia Huang, Xiaoli Chen, Renmin Ni, Qingxue Zhang, Dongzi Yang, Yu Li
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2023-06-01
coleção:	Journal of Ovarian Research
Assuntos:	17α-hydroxylase/17,20-lyase deficiency Congenital adrenal hyperplasia Infertility Pregnancy Assisted reproductive technique
Acesso em linha:	https://doi.org/10.1186/s13048-023-01190-6
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!