Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 명기범 | * |
dc.contributor.author | 최혜영 | * |
dc.date.accessioned | 2018-06-06T08:13:14Z | - |
dc.date.available | 2018-06-06T08:13:14Z | - |
dc.date.issued | 2005 | * |
dc.identifier.issn | 0494-4739 | * |
dc.identifier.other | OAK-17463 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/244720 | - |
dc.description.abstract | Netherton Syndrome is a rare autosomal recessive inherited disorder, characterized by triad of congenital ichthyosiform dermatosis, trichorrhexis invaginata and atopy diathesis. It has been found to be due to mutations in SPINK5, a gene encoding LEKTI (lympho-epithelial Kazal-type related inhibitor). LEKTI is a serine proteinase inhibitor that is expressed in epithelial and lymphoid tissues, and may be important in the keratinocyte terminal differentiation and T and B cell maturation. We herein report two cases of Netherton Syndrome in sisters who had ichthyosis linearis circumflexa, trichorrhexis invaginata and atropic dermatitis. | * |
dc.language | Korean | * |
dc.title | Netherton Syndrome in two sisters | * |
dc.type | Article | * |
dc.relation.issue | 3 | * |
dc.relation.volume | 43 | * |
dc.relation.index | SCOPUS | * |
dc.relation.index | KCI | * |
dc.relation.startpage | 379 | * |
dc.relation.lastpage | 382 | * |
dc.relation.journaltitle | Korean Journal of Dermatology | * |
dc.identifier.scopusid | 2-s2.0-18944389496 | * |
dc.author.google | So Y.K. | * |
dc.author.google | Myung H.K. | * |
dc.author.google | Hae Y.C. | * |
dc.author.google | Ki B.M. | * |
dc.contributor.scopusid | 명기범(7006220296) | * |
dc.contributor.scopusid | 최혜영(55724363200) | * |
dc.date.modifydate | 20231116122502 | * |