• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[伴有指甲改变的疣状表皮发育不良样遗传性皮肤病]

[Epidermodysplasia verruciformis-like genodermatosis with changes in the nails].

作者信息

Salamon T, Halepović E, Berberović L, Nikulin A, Lazović-Tepavac O, Cerkez A, Basić V

机构信息

Lehrstuhl für Dermatologie und Venerologie, Medizinischen Fakultät, Universität Banja Luka.

出版信息

Hautarzt. 1987 Sep;38(9):525-31.

PMID:3692854
Abstract

Nine cases of genodermatosis are described, in which the clinical symptoms and light-microscope findings resembled those in epidermodysplasia verruciformis (Lewandowsky-Lutz disease). All had alterations of the fingernails and toenails. Viruses were not found in a excised skin lesions or in the fingernail clipping from the patients. The mode of inheritance of the dermatosis seems to be X-chromosomal and dominant. It is the opinion of the authors that this dermatosis is separate entity from epidermodysplasia verruciformis.

摘要

本文描述了9例遗传性皮肤病患者,其临床症状和光学显微镜检查结果与疣状表皮发育不良(Lewandowsky-Lutz病)相似。所有患者均有指甲和趾甲改变。在切除的皮肤病变组织或患者的指甲剪屑中均未发现病毒。该皮肤病的遗传方式似乎为X染色体显性遗传。作者认为,这种皮肤病是一种有别于疣状表皮发育不良的独立疾病。

相似文献

1
[Epidermodysplasia verruciformis-like genodermatosis with changes in the nails].[伴有指甲改变的疣状表皮发育不良样遗传性皮肤病]
Hautarzt. 1987 Sep;38(9):525-31.
2
Homozygosity for the c.917A→T (p.N306l) polymorphism in the EVER2/TMC8 gene of two sisters with epidermodysplasia verruciformis Lewandowsky-Lutz originally described by Wilhelm Lutz.两位曾被 Wilhelm Lutz 描述为寻常疣状表皮发育不良的姐妹,其 EVER2/TMC8 基因中的 c.917A→T (p.N306l) 多态性纯合。
Dermatology. 2011 Feb;222(1):81-6. doi: 10.1159/000322536. Epub 2010 Dec 29.
3
Four familial cases of epidermodysplasia verruciformis: mother and three sons.
Dermatol Online J. 2009 Apr 15;15(4):8.
4
Autosomal dominant epidermodysplasia verruciformis lacking a known EVER1 or EVER2 mutation.缺乏已知EVER1或EVER2突变的常染色体显性疣状表皮发育不良
Pediatr Dermatol. 2009 May-Jun;26(3):306-10. doi: 10.1111/j.1525-1470.2008.00853.x.
5
[Epidermodysplasia verruciformis: clinicaland epidemiological features of 45 cases in the Department of Dermatology at the University Hospital Center of Yalgado Ouedraogo, Ouagadougou].[疣状表皮发育不良:瓦加杜古亚尔加杜古大学医院中心皮肤科45例临床及流行病学特征]
Dakar Med. 2007;52(2):90-4.
6
Evidence for a nonallelic heterogeneity of epidermodysplasia verruciformis with two susceptibility loci mapped to chromosome regions 2p21-p24 and 17q25.疣状表皮发育不良存在非等位基因异质性的证据,两个易感基因座定位于染色体区域2p21-p24和17q25。
J Invest Dermatol. 2000 Jun;114(6):1148-53. doi: 10.1046/j.1523-1747.2000.00996.x.
7
Autosomal dominant epidermodysplasia verruciformis: a clinicotherapeutic experience in two cases.常染色体显性遗传性疣状表皮发育不良:两例临床治疗经验。
Indian J Dermatol Venereol Leprol. 2010 Sep-Oct;76(5):557-61. doi: 10.4103/0378-6323.69092.
8
[Scattered papules in three Togolese children from a consanguineous marrige: epidermodysplasia verruciformis].[来自近亲婚姻家庭的三名多哥儿童身上出现的散在丘疹:疣状表皮发育不良]
Med Trop (Mars). 2009 Jun;69(3):293-4.
9
[Anatomo-clinical, immunological and developmental profile of Lewandowsky-Lutz epidermodysplasia verruciformis. Literature review apropos of 2 case reports].[疣状表皮发育不良 Lewandowsky-Lutz 型的解剖临床、免疫学及发育特征。关于 2 例病例报告的文献综述]
Rev Med Liege. 1994 Aug 1;49(8):446-51.
10
Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis.两个相邻新基因的突变与疣状表皮发育不良相关。
Nat Genet. 2002 Dec;32(4):579-81. doi: 10.1038/ng1044. Epub 2002 Nov 11.