期刊文献+

新生儿先天性肾上腺皮质增生症三例

原文传递
导出
摘要 病例1:患儿,男,16d,因“皮肤黄染13d”入院。系第2胎第1产,足月顺产,出生体重3500g。生后混合喂养,患儿第3天出现颜阿部皮肤黄染,逐渐加重,蔓延周身,体重增K缓慢。出,1i后尤发热,无呕吐及腹泻,无惊厥。
出处 《中国小儿急救医学》 CAS 2014年第4期256-257,共2页 Chinese Pediatric Emergency Medicine
  • 相关文献

参考文献7

  • 1Trapp CM, Oberfield SE. Recommendations for treatment of non- classic congenitle adrenal hyperplasia (NCCAH) :an update [ J ]. Steroids,2012,77 ( 4 ) : 342 -346.
  • 2宁岩,韩军,武辉,严超英.先天性肾上腺皮质增生症1例[J].中国实用儿科杂志,2013,28(4):311-312. 被引量:3
  • 3Nimkarn S, New MI. Prenatal diagnosis and treatment of congen- ital adrenal hyperplasia due to 21-hydroxylase deficiency [ J 1. Mol Cell Endocrino1,2009,300 ( 1-2 ) : 192-196.
  • 4Allen DB, Hoffman GL, Fitzpatrick P, et al. Improved precision of newborn screening for congenital adrenal hyperplasia using weight-adjusted criteria for 17-hydroxyprogesterone levels [ J ]. J Pediatr, 1997,130 ( 1 ) : 128-133.
  • 5Gruneiro-Papendieck L, Prieto L, Chiesa A, et al. Neonatal screening program for congenital adrenal hyperplasia:adjustments to the recall protocol [ J 1. Horm Res,2001,55 ( 6 ) : 271-277.
  • 6Koh JW, Kim GH, Yoo HW, et al. Clinical features of congenital adrenal insufficiency including growth patterns and significance of ACTH stimulation test: J]. J Korean Med Sci,2013,28 ( 11 ) : 1650-1656.
  • 7Nordenstrom A,Thilen A, Hagenfeldt L, et al. Genotyping is a valuable diagnostic complement to neonatal screening for congen- ital adrenal hyperplasia due to steroid 21-hydroxylase deficiency [ J 1. J Clin Endocrinol Metab, 1999,84 ( 5 ) : 1505 -1509.

二级参考文献7

共引文献2

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