Epidermolysis Bullosa and Aplasia Cutis
Epidermolysis Bullosa and Aplasia Cutis
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大疱性表皮松解症和皮肤发育不全
DOI：
--
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发表时间：
1991
影响因子：
3.6
通讯作者：
F. Powell
中科院分区：
文献类型：
--
作者：
Madeline A. McCarthy;T. Clarke;F. Powell
翻译后摘要：隐性营养不良性表皮大疱性皮肤发育不全发生在一个男婴。这两个罕见的条件的协会进行审查。有报告称，在几种不同类型的大疱性表皮病患者中，同时存在大面积先天性皮肤缺失，特别是下肢皮肤缺失，这表明这些患者的先天性皮肤缺失区域是大疱性疾病的初始表现，而不是一个独特的实体。
Abstract: Recessive dystrophic epidermolysis bullosa with aplasia cutis occurring in a male infant is described. The association of these two rare conditions is reviewed. Reports of the concurrence of large areas of congenital absence of skin, particularly on the lower limbs, in patients with several different types of epidermolysis bullosa suggest that areas of congenital absence of skin in these patients are an initial manifestation of the bullous disease rather than a distinctive entity.
大疱性表皮松解症：当皮肤破裂时。
DOI：
10.1016/s0022-3476(89)80550-5
发表时间：
1989
期刊：
The Journal of pediatrics
影响因子：
--
作者：
Lin,AN;Carter,DM
通讯作者：
Carter,DM