Inherited Bullous Diseases

被引:0
|
作者
Karaduman, Aysen [1 ]
机构
[1] Hacettepe Univ, Tip Fak, Dermatoloji Anabilim Dali, Ankara, Turkey
关键词
Bullous diseases; epidermolysis bullosa; kindler syndrome; DYSTROPHIC EPIDERMOLYSIS-BULLOSA; EXTRACUTANEOUS MANIFESTATIONS; IGA NEPHROPATHY; COMPLICATIONS; CLASSIFICATION; PATHOGENESIS; INVOLVEMENT; DIAGNOSIS; RISK; EB;
D O I
10.4274/turkderm.45.s14
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Epidermolysis bullosa (EB), refers to a group of inherited bullous disorders, characterized by fagility of the skin and mucous membranes, and blister formation in response to minor friction or trauma. Skin fragility and bulla formation of EB result from genetic mutations of any of dozen genes that encode structural proteins which normally reside within the epidermis, the dermo-epidermal juntion, or the upper dermis. There are four major type of inherited epidermolysis bullosa: EB simplex (EBS), junctional EB (JEB), dystrophic EB (DEB) and Kindler syndrome. (Turkderm 2011; 45 Suppl 2: 81-6)
引用
收藏
页码:81 / 86
页数:6
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