Full-term live birth in a woman with 17α-hydroxylase and 17,20-lyase deficiency with assisted reproductive technology: a case report

BACKGROUND: 17α-hydroxylase deficiency, which is caused by a CYP17A1 gene mutation, is a rare type of congenital adrenocortical hyperplasia that mainly manifests as hypertension, hypokalaemia and sexual dysplasia. To date, few pregnancies associated with this syndrome have been reported. CASE PRESEN...

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Detalles Bibliográficos
Autores principales: Xi, Sisi, Yang, Xiuli, Shan, Xuemin, Xue, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401783/
https://www.ncbi.nlm.nih.gov/pubmed/37542252
http://dx.doi.org/10.1186/s12905-023-02492-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401783/
https://www.ncbi.nlm.nih.gov/pubmed/37542252
http://dx.doi.org/10.1186/s12905-023-02492-z

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