• 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.

作者信息

Pang S Y, Pollack M S, Marshall R N, Immken L

机构信息

Department of Pediatrics, College of Medicine, University of Illinois, Chicago 60612.

出版信息

N Engl J Med. 1990 Jan 11;322(2):111-5. doi: 10.1056/NEJM199001113220207.

DOI:10.1056/NEJM199001113220207
PMID:2403652
Abstract
摘要

相似文献

1
Prenatal treatment of 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的产前治疗。
N Engl J Med. 1990 Jan 11;322(2):111-5. doi: 10.1056/NEJM199001113220207.
2
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.
3
[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.
4
[Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].[21-羟化酶缺乏所致肾上腺增生:产前诊断与治疗。新生儿诊断]
Rev Med Liege. 1986 Jan 15;41(2):37-44.
5
Maternal side effects of prenatal dexamethasone therapy for fetal congenital adrenal hyperplasia.
J Clin Endocrinol Metab. 1992 Jul;75(1):249-53. doi: 10.1210/jcem.75.1.1619017.
6
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.
7
Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
Ann N Y Acad Sci. 1985;458:111-29. doi: 10.1111/j.1749-6632.1985.tb14597.x.
8
Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21-hydroxylase deficiency.21-羟化酶缺乏症女性胎儿的产前诊断及成功的宫内治疗
Med J Aust. 1992 Jan 20;156(2):132-5.
9
Comments about the need for prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.关于21-羟化酶缺乏所致先天性肾上腺皮质增生症产前治疗必要性的评论。
J Clin Endocrinol Metab. 1990 Apr;70(4):836-7. doi: 10.1210/jcem-70-4-836.
10
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.

引用本文的文献

1
Advancing precision care in pregnancy through a treatable fetal findings list.通过一份可治疗的胎儿检查结果清单推进孕期精准护理。
Am J Hum Genet. 2025 Jun 5;112(6):1251-1269. doi: 10.1016/j.ajhg.2025.03.011. Epub 2025 Apr 9.
2
Early dexamethasone treatment induces placental apoptosis in sheep.早期地塞米松治疗可诱导绵羊胎盘细胞凋亡。
Reprod Sci. 2015 Jan;22(1):47-59. doi: 10.1177/1933719114542028. Epub 2014 Jul 25.
3
Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8.
导致先天性肾上腺皮质增生症和高血压的CYP11B1基因突变集中在外显子6、7和8中。
Proc Natl Acad Sci U S A. 1993 May 15;90(10):4552-6. doi: 10.1073/pnas.90.10.4552.
4
Fetal drug therapy.胎儿药物治疗。
West J Med. 1993 Sep;159(3):325-32.
5
Successful prenatal treatment of 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的成功产前治疗。
Eur J Pediatr. 1994 Aug;153(8):556-9. doi: 10.1007/BF02190657.
6
Prenatal diagnosis of enzyme defects--an update.酶缺陷的产前诊断——最新进展
Arch Dis Child. 1991 Apr;66(4 Spec No):451-4. doi: 10.1136/adc.66.4_spec_no.451.
7
TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiency.TaqI HLA - B和 - DRB限制性片段长度多态性分析能够预测患有21 - 羟化酶缺乏症的患病儿童同胞的疾病情况。
Hum Genet. 1990 Oct;85(5):467-72. doi: 10.1007/BF00194218.