目的：探讨大疱性表皮松解型药疹的发生特点及一般规律。
Objective: Analysis characteristic and regularity of epidermolysis bullosa type eruption.
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.
文章摘要：目的对伴有斑点状色素沉着的单纯型大疱性表皮松解症一个家系进行基因检测，明确其病因及基因突变位点。
Abstr: Objective To determine the diagnosis and underlying gene mutation in a large Chinese family with epidermolysis bullosa simplex with mottled pigmentation.
目的：探讨大疱性表皮坏死松解型药疹的临床特征及治疗效果以指导今后临床。
Objective: to analyze the clinical features and therapeutic effects on bullous epidermal necrolysis type drug eruption in order to improve clinical management of the disease.
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.
皮肤病理活检示棘刺松解性大疱，直接免疫荧光棘细胞间及基底膜区免疫反应物沉积，其免疫组化示T细胞侵入表皮现象。
IgG and C 3 can be seen intercellular and in basement membrane zone by direct immunofluorescence. The immune -histochemistry showed that there was T cell infiltration into epidermis.
皮肤病理活检示棘刺松解性大疱，直接免疫荧光棘细胞间及基底膜区免疫反应物沉积，其免疫组化示T细胞侵入表皮现象。
IgG and C 3 can be seen intercellular and in basement membrane zone by direct immunofluorescence. The immune -histochemistry showed that there was T cell infiltration into epidermis.
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