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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

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