期刊文献+

婴儿Netherton综合征一例 被引量:1

下载PDF
导出
摘要 Netherton综合征是一种由SPINK5基因突变导致的严重且少见的常染色体隐形遗传病,估计全世界发病率约为1/200000[1]。目前该病全世界范围报道相对较少,尤其国内,现将收集一例婴儿Netherton综合征报道如下.
出处 《海南医学》 CAS 2020年第7期942-944,共3页 Hainan Medical Journal
  • 相关文献

参考文献3

二级参考文献37

  • 1Hausser I,Anton-Lampre cht I.Severe congenital generalizedexfoliative erythroderma in newborns and infants:a possible signof Netherton syndrome.Pediatr Dennatol,1996,13(3):183-199.
  • 2Bennett K,Heywood Wi Di WL,et al.The identification of anew role for LEKTI in the skin:The use of protein "baity arraysto detect defective trafficking of dermcidin in the skin of patientswith Netherton syndrome.J Proteomics,2012,75(13):3925-3937.
  • 3Descargues P,Deraison C,Prost C,et al.Comeodesmosomalcadherins are preferential targets of stratum corneum trypsin-andchymotrypsin-like hyperactivity in Netherton syndrome.J InvestDermatol,2006,126(7):1622-1632.
  • 4Hachem JP,Wagberg F,Schmuth M,et al.Serine proteaseactivity and residual LEKTI expression determine phenotype inNetherton syndrome.J Invest Dermatol,2006,126(7):1609-1621.
  • 5Chavanas S,Bodemer C,Rochat A,et al.Mutations in SPINK5,encoding a serine protease inhibitor,cause Netherton syndrome.Nat Genet,2000,25(2):141-142.
  • 6Mitsudo K,Jayakumar A,Henderson Y,et al.Inhibition of serineproteinases plasmin,trypsin,subtilisin A,cathepsin G,andelastase by LEKTI:a kinetic analysis.Biochemistry,2003,42(13):3874-3881.
  • 7Deraison C,Bonnart C,Lopez F,et al.LEKTI fragmentsspecifically inhibit KLK5,KLK7,and KLK14 and controldesquamation through a pH-dependent interaction.Mol Biol Cell,2007,18(9):3607-3619.
  • 8Descargues P,Deraison C,Bonnart C,et al.Spink5-deficientmice mimic Netherton syndrome through degradation ofdesmoglein I by epidermal protease hyperactivity.Nat Genet,2005,37(1):56-65.
  • 9Bitoun E,Micheloni A,Lamant L,et al.LEKTI proteolyticprocessing in human primary keratinocytes,tissue distributionand defective expression in Netherton syndrome.Hum MolGenet,2003,12(19):2417-2430.
  • 10Xi-Bao Z,San-Quan Z,Yu-Qing H,et al.Netherton syndrome inone Chinese adult with a novel mutation in the SPINK5 gene andimmunohistochemical studies of LEKTI.Indian J Dermatol,2012,57(4):265-268.

共引文献11

同被引文献8

引证文献1

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