epidermolysis
[医] 表皮松解
常用释义
英音[ epɪdəˈmɒləsɪs ]
美音[ epɪdərˈmɔːləsɪs ]
基本释义
- n. [医] 表皮松解
例句
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1·Objective: Analysis characteristic and regularity of epidermolysis bullosa type eruption.目的：探讨大疱性表皮松解型药疹的发生特点及一般规律。
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2·Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis.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。
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3·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。
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4·Objective:To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.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。
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5·Objective to investigate the experience of the specialized nursing of toxic epidermolysis, improve specialized nursing care and accelerate patients get well soon.目的总结中毒性表皮松解症(TEN)患者的护理经验，提高护理质量，有效地促进患者康复。
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6·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.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。
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7·Conclusions The splicing mutation of COL7A1 gene is the underlying cause of and specific rather than common polymorphism for the family with dystrophic epidermolysis bullosa pruriginosa subtype.结论COL7A1基因剪接位点的突变是引起该家系临床症状的特异突变，而非多态性改变。