Dexamethasone application for in vitro fertilisation in non-classic 17-hydroxylase/17,20-lyase-deficient women

Dexamethasone application for in vitro fertilisation in non-classic 17-hydroxylase/17,20-lyase-deficient women

ContextHigh progesterone levels in the follicular stage interfere with the implantation window, causing infertility in women with 17-hydroxylase/17,20-lyase deficiency (17OHD). Dexamethasone can restore cortisol deficiency and suppress inappropriate mineralocorticoid secretion to control hypertensio...

Full description

Bibliographic Details
Main Authors:	Xiu-Li Yang, Ting-Ting Zhang, Jing Shang, Qing Xue, Yan-Rong Kuai, Sheng Wang, Yang Xu
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2022-10-01
Series:	Frontiers in Endocrinology
Subjects:	17-hydroxylase/17,20-lyase deficiency dexamethasone infertility in vitro fertilization pregnancy
Online Access:	https://www.frontiersin.org/articles/10.3389/fendo.2022.971993/full

Similar Items

Functional Identification of Compound Heterozygous Mutations in the Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency
by: Eun Yeong Mo, et al.
Published: (2018-09-01)

Endocrine profiles and cycle characteristics of infertile 17α-hydroxylase/17,20-lyase Deficiency Patients undergoing assisted Reproduction Treatment: a retrospective cohort study
by: Ping Pan, et al.
Published: (2023-06-01)

Full-term live birth in a woman with 17α-hydroxylase and 17,20-lyase deficiency with assisted reproductive technology: a case report
by: Sisi Xi, et al.
Published: (2023-08-01)

A novel homozygous CYP17A1 mutation causes partial 17 α-hydroxylase/17,20-lyase deficiency in 46,XX: a case report and literature review
by: Heye Chen, et al.
Published: (2023-12-01)

New insights on hyperglycemia in 17-hydroxylase/17,20-lyase deficiency
by: Lingling Xu, et al.
Published: (2022-07-01)

A patient with primary amenorrhoea and hypertension: 17 á hydroxylase deficiency – a rare cause of congenital adrenal hyperplasia
by: W. C. K. Jayawardena, et al.
Published: (2010-07-01)

Ovarian gonadoblastoma with dysgerminoma in a girl with 46,XX karyotype 17a-hydroxylase/17, 20-lyase deficiency: A case report and literature review
by: Min Yin, et al.
Published: (2022-12-01)

An Asian case of combined 17α-hydroxylase/17,20-lyase deficiency due to homozygous p.R96Q mutation: A case report and review of the literature
by: Qian Liao, et al.
Published: (2022-10-01)

Clinical and Genetic Analysis of a Patient With Coexisting 17a-Hydroxylase/17,20-Lyase Deficiency and Moyamoya Disease
by: Jiaming Huang, et al.
Published: (2022-08-01)

Congenital Adrenal Hyperplasia due to 17-alpha-hydoxylase/17,20-lyase Deficiency Presenting with Hypertension and Pseudohermaphroditism: First Case Report from Oman
by: Waad-Allah S. Mula-Abed, et al.
Published: (2014-01-01)

Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation
by: Hae In Lee, et al.
Published: (2021-03-01)

Pregnancy outcomes in in vitro fertilization in 17-alpha-hydroxylase deficiency
by: Annika van Oosbree, M.S.-IV, et al.
Published: (2023-06-01)

17-α-Hydroxylase deficiency: An unusual case with primary amenorrhea and hypertension
by: Sunil Kumar Kota, et al.
Published: (2011-01-01)

Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
by: Menglin Wang, et al.
Published: (2019-10-01)

Severe hypertension caused by 17α-hydroxylase deficiency: A case report
by: YaJing Zhao, et al.
Published: (2023-03-01)

17 alpha‐hydroxylase deficiency: A case report of young Chinese woman with a rare gene mutation
by: Li Hui Han, et al.
Published: (2022-07-01)

Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients
by: Duoduo Zhang, et al.
Published: (2022-12-01)

Refractory hypokalemia with sexual dysplasia and infertility caused by 17α-hydroxylase deficiency and triple X syndrome: A case report
by: Yao Jun-Teng, et al.
Published: (2023-02-01)

Successful Treatment of Infertility in a Patient with Probable 17 Hydroxylase Deficiency and Particularities of Association with Adrenal Autoimmunity—A Case Report and Review of the Literature
by: Alice Ioana Albu, et al.
Published: (2023-03-01)

Case report: 17α− hydroxylase deficiency due to a hotspot variant and a novel compound heterozygous variant in the CYP17A1 gene of five Chinese patients
by: Jinying Li, et al.
Published: (2022-09-01)

Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
by: Yukiko Mikami, et al.
Published: (2019-07-01)

Case report: Management challenges of late diagnosed 17‐alpha hydroxylase deficiency
by: Dhoha Ben Salah, et al.
Published: (2023-02-01)

Biochemical Characterization and Cold-Adaption Mechanism of a PL-17 Family Alginate Lyase Aly23 from Marine Bacterium <i>Pseudoalteromonas</i> sp. ASY5 and Its Application for Oligosaccharides Production
by: Xiang Tang, et al.
Published: (2022-02-01)

Understanding neuroendocrine regulatory pathways of sexual behavior in teleosts
by: Saokat Ahamed, et al.
Published: (2024-05-01)

Seventeen Alpha-hydroxylase Deficiency
by: Siew-Lee Wong, et al.
Published: (2006-01-01)

Flash glucose monitoring system was applied to cortisol treatment for a patient with congenital adrenal hyperplasia and 17α-hydroxylase deficiency
by: Chenyu Xiang, et al.
Published: (2020-09-01)

Hiperplasia suprarrenal congénita, deficiencia de 17-alfa-hidroxilasa/17,20-liasa: reporte de caso
by: Luis M. López-Solorzano, et al.
Published: (2022-04-01)

Multiple 17-OHP Cutoff Co-Variates Fail to Improve 21-Hydroxylase Deficiency Screening Accuracy
by: Preet K. Matharu, et al.
Published: (2022-10-01)

SRT1720 Alleviates ANIT-Induced Cholestasis in a Mouse Model
by: Linxi Yu, et al.
Published: (2017-05-01)

Reproductive endocrine characteristics and in vitro fertilization treatment of female patients with partial 17α-hydroxylase deficiency: Two pedigree investigations and a literature review
by: Shutian Jiang, et al.
Published: (2022-09-01)

First Morning Pregnanetriol and 17-Hydroxyprogesterone Correlated Significantly in 21-Hydroxylase Deficiency
by: Tomoyo Itonaga, et al.
Published: (2022-01-01)

SRT1720 as an SIRT1 activator for alleviating paraquat-induced models of Parkinson's disease
by: Chih-Chang Chao, et al.
Published: (2022-12-01)

IL-17-producing double-negative T cells are expanded in the peripheral blood, infiltrate the salivary gland and are partially resistant to corticosteroid therapy in patients with Sjögren’s syndrome
by: A. Alunno, et al.
Published: (2013-10-01)

Serum and seminal plasma levels of interleukin-17 in infertile patients
by: Abdelrahman A. Elsaied, et al.
Published: (2024-01-01)

Th17-Dependent Nasal Hyperresponsiveness Is Mitigated by Steroid Treatment
by: Shusaku Ueda, et al.
Published: (2022-05-01)

Role of interleukin 17 (IL-17) in the inflammatory hypothesis of depression
by: Katarzyna Bliźniewska-Kowalska, et al.
Published: (2023-12-01)

Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: laboratory criteria for the diagnosis and control of treatment efficacy
by: O.V. Rykova
Published: (2019-08-01)

Variation in serum adrenal hormones in female 21-hydroxylase deficient patients
by: Ditte Sofie Dahl Sørensen, et al.
Published: (2022-06-01)

Epinephrine Production in Th17 Cells and Experimental Autoimmune Encephalitis
by: Pinguang Yang, et al.
Published: (2021-02-01)

IL-17C/IL-17RE: Emergence of a Unique Axis in TH17 Biology
by: Jasper F. Nies, et al.
Published: (2020-02-01)