期刊文献+

先天性肾上腺皮质增生症21-羟化酶缺陷的非孕期合理管理

下载PDF
导出
摘要 先天性肾上腺皮质增生症(congenital adrenal hyperplasia,CAH)是一组由于肾上腺皮质激素合成酶基因突变导致酶活性缺乏或减低,肾上腺皮质激素合成减少,负反馈引起促肾上腺皮质激素(adrenocorticotropic hormone,ACTH)水平升高,继发肾上腺增生的疾病。
作者 翁妍 张少玲
出处 《实用妇产科杂志》 CAS CSCD 北大核心 2021年第6期403-406,共4页 Journal of Practical Obstetrics and Gynecology
基金 国家自然科学基金(编号:81970683) 广东省自然科学基金(编号:2020A1515010245)。
  • 相关文献

二级参考文献56

  • 1Speiser PW, Azziz R, Baskin LS, et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency : Endocrine Society clinical practice guideline [ J ]. J Clin Endocrinol Metab, 2010, 95 (9) : 41334160. DOI: 10. 1210/ jc. 2009-2631.
  • 2Miller WL. Moleeular biology of steroid hormone synthesis [ J]. Endoer Rev, 1988, 9(3) :295-318.
  • 3Gidl6f S, Wedell A, Guthenberg C, et al. Nationwide neonatal screening for congenital adrenal hyperplasia in sweden a 26-year longitudinal prospective population-based study [ J ]. JAMA Pediatr, 2014, 168 ( 6 ): 567-574. DOI: 10. 1001/ jamapediatries. 2013. 5321.
  • 4Sharma R, Seth A. Congenital adrenal hyperplasia: issues in diagnosis and treatment in children[ J]. Indian J Pediatr, 2014, 81 : (2) :178-185. DOI: 10. 1007/s120984313-1280-8.
  • 5Forest MG. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency [J]. Hum Reprod Update, 2004,10(6) :469-485.
  • 6Huynh T, McGown I, Cowley D, et al. The clinical and biochemical spectrum of congenital adrenal hyperplasia secondap/ to 21-hydroxylase deficiency [ J ]. Cfin Biochem Rev, 2009, 30 (2) :75-86.
  • 7Balsamo A, Baldazzi L, Menabb S, et al. Impact of molecular genetics on congenital adrenal hyperplasia management [ J]. Sex Dev, 2010, 4(4-5) :233-248. DOI: 10. 1159/000315959.
  • 8Forest MG. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency[J].Hum Reprod Update, 2004,10(6):469-485.
  • 9Balsamo A, Cacciari E, Baldazzi L, et al. CYP21 analysis and phenotype/genotype relationship in the screened population of the Italian Emilia-Romagna region [ J ]. Clin Endocrinol ( Oxf), 2000, 53(1) :117-125.
  • 10Padidela, R, Hindmarsh PC. Mineralocorticoid deficiency and treatment in congenital adrenal hyperplasia [ J ]. Int J Pediatr Endocrinol, 2010, 2010:656925. DOI: 10.1155/2010/656925.

共引文献80

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部