金德勒综合征:两例兄弟姐妹的临床特点

Dermatology and Dermatitis Pub Date : 2020-10-21 DOI:10.31579/2578-8949/067

Elharrouni Alaoui A, B. H, C. R, Douhi Z, E. S, Mernissi Fz

{"title":"金德勒综合征:两例兄弟姐妹的临床特点","authors":"Elharrouni Alaoui A, B. H, C. R, Douhi Z, E. S, Mernissi Fz","doi":"10.31579/2578-8949/067","DOIUrl":null,"url":null,"abstract":"The Kindler syndrome, the fourth major type of hereditary epidermolysis bullosa (HEB), is a rare autosomal recessive genodermatoses, characterized by trauma-induced blistering, cutaneous atrophy, and progressive poikiloderma, in association with mucosal inflammation. We report tow new sibling cases of this rare syndrome.","PeriodicalId":350109,"journal":{"name":"Dermatology and Dermatitis","volume":"21 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Kindler Syndrome : Clinical Particularities about Two Cases Reports in Two Siblings\",\"authors\":\"Elharrouni Alaoui A, B. H, C. R, Douhi Z, E. S, Mernissi Fz\",\"doi\":\"10.31579/2578-8949/067\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The Kindler syndrome, the fourth major type of hereditary epidermolysis bullosa (HEB), is a rare autosomal recessive genodermatoses, characterized by trauma-induced blistering, cutaneous atrophy, and progressive poikiloderma, in association with mucosal inflammation. We report tow new sibling cases of this rare syndrome.\",\"PeriodicalId\":350109,\"journal\":{\"name\":\"Dermatology and Dermatitis\",\"volume\":\"21 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-10-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dermatology and Dermatitis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31579/2578-8949/067\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dermatology and Dermatitis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31579/2578-8949/067","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 0

摘要

Kindler综合征是遗传性大疱性表皮松解症(HEB)的第四种主要类型，是一种罕见的常染色体隐性遗传性皮肤病，其特征是外伤性起泡、皮肤萎缩和进行性千皮病，并伴有粘膜炎症。我们报告两个新的兄弟病例这种罕见的综合征。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Kindler Syndrome : Clinical Particularities about Two Cases Reports in Two Siblings

The Kindler syndrome, the fourth major type of hereditary epidermolysis bullosa (HEB), is a rare autosomal recessive genodermatoses, characterized by trauma-induced blistering, cutaneous atrophy, and progressive poikiloderma, in association with mucosal inflammation. We report tow new sibling cases of this rare syndrome.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Dermatology and Dermatitis

自引率

0.00%

发文量