• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a 10 year experience.

作者信息

Forest M G, David M

机构信息

INSERM, U.329, Hôpital Debrousse, Lyon, France.

出版信息

Indian J Pediatr. 1992 Jul-Aug;59(4):515-22. doi: 10.1007/BF02751569.

DOI:10.1007/BF02751569
PMID:1452270
Abstract
摘要

相似文献

1
Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a 10 year experience.
Indian J Pediatr. 1992 Jul-Aug;59(4):515-22. doi: 10.1007/BF02751569.
2
[The effect of maternal dexamethasone treatment after the 12th week of pregnancy on fetal genital development in adrenogenital syndrome with 21-hydroxylase deficiency].妊娠12周后母体地塞米松治疗对21-羟化酶缺乏所致肾上腺生殖器综合征胎儿生殖器发育的影响
Monatsschr Kinderheilkd. 1989 May;137(5):293-6.
3
[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency].[21-羟化酶缺乏所致先天性肾上腺皮质增生症]
Nihon Rinsho. 2004 Feb;62(2):361-7.
4
Hydrometrocolpos following prenatal dexamethasone treatment for congenital adrenal hyperplasia (21-hydroxylase deficiency).先天性肾上腺皮质增生症（21-羟化酶缺乏症）产前地塞米松治疗后出现的阴道积血和子宫积血。
Eur J Pediatr. 1993 Jan;152(1):9-11. doi: 10.1007/BF02072507.
5
Sequential use of hydrocortisone and dexamethasone in prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.氢化可的松与地塞米松序贯用于21-羟化酶缺乏所致先天性肾上腺皮质增生症的产前治疗
Horm Res Paediatr. 2013;79(5):323-4. doi: 10.1159/000351235. Epub 2013 May 25.
6
Prenatal diagnosis and management of congenital adrenal hyperplasia.
Clin Perinatol. 1994 Sep;21(3):631-45.
7
[Familial congenital adrenal hyperplasia caused by 11 beta-hydroxylase. Failure of prevention of sexual ambiguity and prenatal diagnosis].[由11β -羟化酶引起的家族性先天性肾上腺皮质增生症。性器官模糊预防失败及产前诊断]
Pediatrie. 1989;44(8):637-40.
8
Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia.11β-羟化酶缺乏所致先天性肾上腺皮质增生症导致女性生殖器正常的产前诊断与治疗
J Clin Endocrinol Metab. 1999 Sep;84(9):3129-34. doi: 10.1210/jcem.84.9.5976.
9
[Prenatal diagnosis and therapy of adrenogenital syndrome with 21-hydroxylase deficiency].[21-羟化酶缺乏所致肾上腺生殖器综合征的产前诊断与治疗]
Geburtshilfe Frauenheilkd. 1992 Oct;52(10):586-8. doi: 10.1055/s-2007-1023188.
10
[Diagnosis and treatment of fetal congenital adrenal cortex hyperplasia].
Lakartidningen. 1986 Dec 24;83(52):4462-3.

引用本文的文献

1
Experts' Opinion on the Prenatal Therapy of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency - Guideline of DGKED in cooperation with DGGG (S1-Level, AWMF Registry No. 174/013, July 2015).21-羟化酶缺乏所致先天性肾上腺皮质增生症（CAH）产前治疗专家意见——德国儿科内分泌与糖尿病学会（DGKED）与德国儿科学会（DGGG）合作制定的指南（S1级，德国医学科学与医学技术评估机构注册编号174/013，2015年7月）
Geburtshilfe Frauenheilkd. 2015 Dec;75(12):1232-1238. doi: 10.1055/s-0041-109717.
2
Intersex disorder associated with ambiguous genitalia.
Indian J Pediatr. 1992 Jul-Aug;59(4):463-6. doi: 10.1007/BF02751563.

本文引用的文献

1
[The syndrome of male pseudohermaphrodism in congenital adrenocortical hyperplasia without overproduction of androgens (adrenal male pseudohermaphrodism)].先天性肾上腺皮质增生症中无雄激素过度分泌的男性假两性畸形综合征（肾上腺性男性假两性畸形）
Helv Paediatr Acta. 1955 Aug;10(4):397-412.
2
Concentration of 14 steroid hormones in human amniotic fluid of midpregnancy.孕中期人羊水内14种甾体激素的浓度
J Clin Endocrinol Metab. 1980 Oct;51(4):816-22. doi: 10.1210/jcem-51-4-816.
3
Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency.
21-羟化酶缺乏所致先天性肾上腺皮质增生症的产前治疗。
J Pediatr. 1984 Nov;105(5):799-803. doi: 10.1016/s0022-3476(84)80310-8.
4
A possible new HLA-DR allele.一种可能的新的人类白细胞抗原-DR等位基因。
Hum Immunol. 1983 Nov;8(3):227-37. doi: 10.1016/0198-8859(83)90040-x.
5
Pitfalls in prenatal diagnosis of 21-hydroxylase deficiency by amniotic fluid steroid analysis? A six years experience in 102 pregnancies at risk.通过羊水类固醇分析进行21-羟化酶缺乏症的产前诊断存在哪些陷阱？对102例有风险妊娠的六年经验总结。
Ann N Y Acad Sci. 1985;458:130-47. doi: 10.1111/j.1749-6632.1985.tb14598.x.
6
Genetics of adrenal steroid 21-hydroxylase deficiency.肾上腺类固醇21-羟化酶缺乏症的遗传学
Endocr Rev. 1986 Aug;7(3):331-49. doi: 10.1210/edrv-7-3-331.
7
Successful prenatal treatment of congenital adrenal hyperplasia resulting from the 21-hydroxylase deficiency: is prenatal diagnosis in a mother at risk essential?
Endokrynol Pol. 1987;38(1):125-30.
8
Molecular and clinical advances in congenital adrenal hyperplasia.先天性肾上腺皮质增生症的分子与临床进展
J Pediatr. 1987 Jul;111(1):1-17. doi: 10.1016/s0022-3476(87)80334-7.
9
Prenatal treatment in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: up-date 88 of the French multicentric study.21-羟化酶缺乏所致先天性肾上腺皮质增生症的产前治疗：法国多中心研究的第88次更新
Endocr Res. 1989;15(1-2):277-301. doi: 10.1080/07435808909039101.
10
Prenatal treatment of congenital adrenal hyperplasia: report of a new case.先天性肾上腺皮质增生症的产前治疗：1例新病例报告
Eur J Pediatr. 1990 Jan;149(4):237-40. doi: 10.1007/BF02106280.