国际DebRA组织资助的基因研究 大疱性表皮松解症(Epidermolysis Bullosa, EB)是一种基因疾病,大约17,000个新生儿中有一个受影响。英国估计有4到5,000人患病,全球估计为3
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获得性大疙性表皮松解症(epidermolysis bullesa acguisita )为少见的非遗传性慢性大疙性皮肤病,可能是一种自身免疫性疾病。表现为外伤部位出现表皮下水疤。
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大疱性表皮松解症 epidermolysis bullosa ; DEB ; epidermolysis bullosa hereditaria ; EB
性大疱性表皮松解症 DDEB
单纯性表皮松解症 epidermolysis simplex
疱性表皮松解症 Jonctional EB ; Epidermolysis bullosa ; JEB
大庖性表皮松解症 [皮肤] epidermolysis bullosa
中毒性表皮坏死松解症 toxic epidermal necrolysis ; TEN ; staphylococcal toxic epidermal necrolysis
大疱性表皮坏死松解症 bullous epidermal necrolysis ; Epidermolysis Bullosa
其他大疱性表皮松解症 Other epidermolysis bullosa
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.
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