Reproductive endocrine characteristics and in vitro fertilization treatment of female patients with partial 17α-hydroxylase deficiency: Two pedigree investigations and a literature review

BACKGROUND: 17α-hydroxylase/17, 20-lyase deficiency (17-OHD) is caused by the mutations of the CYP17A1 gene. The classical phenotype of 17-OHD includes hypertension, hypokalemia, and abnormal sexual development, with partial 17-OHD typically less severe than the complete deficiency. Infertility is a...

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Detalles Bibliográficos
Autores principales: Jiang, Shutian, Xu, Yue, Qiao, Jie, Wang, Yao, Kuang, Yanping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516945/
https://www.ncbi.nlm.nih.gov/pubmed/36187111
http://dx.doi.org/10.3389/fendo.2022.970190

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516945/
https://www.ncbi.nlm.nih.gov/pubmed/36187111
http://dx.doi.org/10.3389/fendo.2022.970190

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