1. Successful live birth in women with partial 17α-hydroxylase deficiency: report of two cases.
- Author
-
Du X, Jia Q, Wu S, Wang B, and Guan Y
- Subjects
- Humans, Female, Adult, Pregnancy, Adrenal Hyperplasia, Congenital drug therapy, Adrenal Hyperplasia, Congenital complications, Embryo Transfer, Infertility, Female therapy, Steroid 17-alpha-Hydroxylase genetics, Fertilization in Vitro methods, Prednisone therapeutic use, Endometrium, Live Birth
- Abstract
Research Question: Can women with partial 17α-hydroxylase deficiency (17-OHD) conceive naturally with adequate hormonal control and endometrial preparation?, Design: This report presents two cases of women with partial 17-OHD who achieved successful pregnancies. The first case involved a 27-year-old Chinese woman with recurrent cysts and infertility, and the second case involved a 32-year-old Chinese woman with a complex disorder requiring IVF. Both cases were treated with oral prednisone to control hormone concentrations and underwent endometrial preparation., Results: In the first case, the patient resumed spontaneous ovulation, conceived naturally, and gave birth to a healthy baby. In the second case, after cryopreserving embryos due to a thin endometrium, the patient underwent frozen embryo transfer and achieved a singleton pregnancy., Conclusion: This study suggests that women with partial 17-OHD can conceive naturally with appropriate hormonal management and endometrial preparation. These findings provide valuable insights into the reproductive potential of women with this disorder, and highlight the importance of further research in this area., (Copyright © 2024 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF