结果：11例重症中毒性大疱性表皮松解症患儿病情痊愈，无溃疡疤痕形成。
Result: 11 cases of toxic epidermal necrolysis patients had completely recovered, without ulcer or scar.
前期的临床实验在治疗创伤，大疱性表皮松解症和鱼鳞病上已经取得了进展。
Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis.
目的：通过透射电镜和免疫荧光研究先天性大疱性表皮松解症患者的基底膜带分子。
Objective:To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.
一种遗传疾病，以先天性局部皮肤缺损、大疱性表皮松解症、口腔粘膜病变、甲营养不良为特征。
Bart syndrome is a genetic disorder characterized by the association of congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails.
儿童获得性大疱表皮松解症（EBA）是一种自身免疫性表皮下大疱病，比较少见。
Epidermolysis bullosa acquisita(EBA) is an autoimmune subepidermal bullous disease. This disease is rare in childhood.
儿童获得性大疱表皮松解症（EBA）是一种自身免疫性表皮下大疱病，比较少见。
Epidermolysis bullosa acquisita(EBA) is an autoimmune subepidermal bullous disease. This disease is rare in childhood.
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