摘要
大疱性表皮松解症(epidermolysis bullosa,EB)是一组较少见的以皮肤和黏膜起疱为特征的遗传性疾病,发生于新生儿期的EB更少见,原因不明。
A spectrum of rare genodermatoses in which a disturbed coherence of the epidermis and/or dermis leads to blister formation following trauma,is especially rare in infant. Pathogenesis is still unknown.
出处
《中国医学文摘（皮肤科学）》
2009年第3期154-,207,共2页
China Medical Abstracts(Dermatology)
