期刊文献+

新生儿肝功能异常和低血糖 被引量:1

原文传递
导出
摘要 住院医师汇报病史患儿,男,16d。2013年7月17日入院,主诉:肝功能异常1周余。患儿系G2P2,孕38+4周,于2013年7月1日在无锡市某医院顺产娩出,出生体重3100g,无窒息抢救史,无胎膜早破,生后2h开奶,吃奶可。生后3d因气急就诊于无锡市某医院,住院治疗13d,期间反复发生低血糖,最低1.3mmol/L。曾因呼吸困难给予持续气道正压通气(CPAP)治疗1d,
作者 张金萍 陈超
出处 《中国小儿急救医学》 CAS 2013年第5期541-542,共2页 Chinese Pediatric Emergency Medicine
  • 相关文献

参考文献6

  • 1Brooks ED, Little D, Arumugam R, et al. Pathogenesis of growth failure and partial reversal with gene therapy in murine and ca- nine Glycogen Storage Disease type la. Mol Genet Metab, 2013, 109(2) : 161 - 170.
  • 2Araoka T,Takeoka H,Abe H, et al. Early diagnosis and treat- ment may prevent the development of complications in an adult patient withglycogen storage disease type Ia. Intern Med, 2010, 49 (16) : 1787 - 1792.
  • 3Carvalho PM, Silva NJ, Dias PG, et ai. Glycogen Storage Disease type 1 a-a secondary cause for hyperlipidemia:report of five ca- ses. J Diabetes Metab Disord,2013,12( 1 ) :25.
  • 4Rake JP, Visser G, Labrune P, et al, Glycoge storage disease type I: diagnosis, management, clinical course and outcome. Results of the European study on glycogen storege disease type I ( ESGSD I). Eur J Pediatr,2002,161 :S20 -S34.
  • 5Roe CR,Ding JH. Mitochondria fatty acid oxidation disorders// Scriver CR, Baudet AL, Valle D, et al. The metabolic and molec- ular bases of inherited disease. 8th edn. New York: NMcGraw- Hill ,2001:2297 - 2326.
  • 6Nagasaka H, Hirano K, Ohtake A, et al. Improvements of hyper- triglyceridemia and hyperlacticemia in Japanese children with glycogen storage disease type la by medium-chain triglyceride milk. Eur J Pediatr ,2007,166 (10) : 1009 - 1016.

同被引文献5

引证文献1

二级引证文献6

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