F Cherif, N Mnajja, S Feriani, Z Marrakchi Ben Saïd, M H Jaafoura, A Ben Osman Dhahri, S Boubaker
{"title":"[突尼斯遗传性大疱性表皮松解症:流行病学、临床和超微结构研究]。","authors":"F Cherif, N Mnajja, S Feriani, Z Marrakchi Ben Saïd, M H Jaafoura, A Ben Osman Dhahri, S Boubaker","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Hereditary epidermolysis bullosa (EB) are a group of genodermatoses whose common primary feature is formation of blisters following minor trauma. The aim of the present study was to assess epidemiological, clinical, genetical and histological particularities of patients with hereditary epidermolysis bullosa.</p>","PeriodicalId":75537,"journal":{"name":"Archives de l'Institut Pasteur de Tunis","volume":"82 1-4","pages":"53-8"},"PeriodicalIF":0.0000,"publicationDate":"2005-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Hereditary epidermolysis bullosa in Tunisia: an epidemio-clinical and ultrastructural study].\",\"authors\":\"F Cherif, N Mnajja, S Feriani, Z Marrakchi Ben Saïd, M H Jaafoura, A Ben Osman Dhahri, S Boubaker\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Hereditary epidermolysis bullosa (EB) are a group of genodermatoses whose common primary feature is formation of blisters following minor trauma. The aim of the present study was to assess epidemiological, clinical, genetical and histological particularities of patients with hereditary epidermolysis bullosa.</p>\",\"PeriodicalId\":75537,\"journal\":{\"name\":\"Archives de l'Institut Pasteur de Tunis\",\"volume\":\"82 1-4\",\"pages\":\"53-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives de l'Institut Pasteur de Tunis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives de l'Institut Pasteur de Tunis","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Hereditary epidermolysis bullosa in Tunisia: an epidemio-clinical and ultrastructural study].
Hereditary epidermolysis bullosa (EB) are a group of genodermatoses whose common primary feature is formation of blisters following minor trauma. The aim of the present study was to assess epidemiological, clinical, genetical and histological particularities of patients with hereditary epidermolysis bullosa.