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

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 manifestation. Ho...

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Detalles Bibliográficos
Autores principales: Pan, Ping, Zheng, Lingyan, Huang, Jia, Chen, Xiaoli, Ni, Renmin, Zhang, Qingxue, Yang, Dongzi, Li, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265862/
https://www.ncbi.nlm.nih.gov/pubmed/37316894
http://dx.doi.org/10.1186/s13048-023-01190-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265862/
https://www.ncbi.nlm.nih.gov/pubmed/37316894
http://dx.doi.org/10.1186/s13048-023-01190-6

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