期刊文献+

假性醛固酮减少症一例报告 被引量:2

原文传递
导出
摘要 假性醛固酮减少症(pseudohypoaldosteronism,PHA)是一种发生于婴儿期的失盐综合征。自从1958年Cheek和Pery报告第一例以后,国外已先后报告了70余例,国内尚罕见报告。现将我院1996年诊治的一例报告如下。患儿男,5月...
出处 《中华内分泌代谢杂志》 CAS CSCD 北大核心 1999年第2期128-128,共1页 Chinese Journal of Endocrinology and Metabolism
  • 相关文献

同被引文献21

  • 1刘男男,张蔚.假性醛固酮减少症1例[J].广东医学,2005,26(3):290-290. 被引量:1
  • 2张爱民,胡朝晖.Ⅰ型假性醛固酮减少症一例[J].医学临床研究,2005,22(7). 被引量:1
  • 3Cheek DB,Perry JW.A salt wasting syndrome in infancy[J].Arch Dis Child,1958,33(169):252-256.
  • 4Schweiger B,Moriarty MW,Cadnapaphornchai MA.Case report:severe neonatal hyperkalemia due to pseudohypoal-dosteronism type 1[J].Curr Opin Pediatr,2009,21(2):269-271.
  • 5Dirlewanger M,Huser D,Zennaro MC,et al.A homozy-gous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1[J].Am J Physiol Endocrinol Metab,2011[Epubahead of print].
  • 6Lee SE,Jung YH,Han KH,et al.A case of pseudohy-poaldosteronism type 1 with a mutation in the mineralocor-ticoid receptor gene[J].Korean J Pediatr,2011,54(2):90-93.
  • 7Belot A,Ranchin B,Fichtner C,et al.Pseudohypoal-dosteronisms,report on a 10-patient series[J].Nephrol Dial Transplant,2008,23:1636-1641.
  • 8Edelheit O,Hanukoglu I,Gizewska M,et al.Novel muta-tions in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoal-dosteronism[J].Clin Endocrinol (Oxf),2005,62(5):547-553.
  • 9Chang SS,Grunder S,Hanukoglu A,et al.Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis,pseudohypoaldoste-ronism type 1[J].Nat Genet,1996,12(3):248-253.
  • 10Schaedel C,Marthinsen L,Kristoffersson AC,et al.Lung symptoms in pseudohypoaldosteronism type 1 are associa-ted with deficiency of the α-subunit of the epithelial sodium channel[J].J Pediatr,1999,135(6):739-745.

引证文献2

二级引证文献8

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