epidermolysis发音

意思翻译

n.[医]表皮松解

相似词语短语

epidermatoid───adj.表皮样的

epidermoid───adj.（生物）表皮样的，像表皮的

outermost layer of the epidermis───表皮的最外层

epidermal sebaceous cyst───表皮皮脂腺囊肿

epidermose───表皮的

epidermal inclusion cyst───表皮包涵囊肿

epidermal setae───表皮刚毛

enepidermic───adj.对皮肤用药的

epidermal growth factor───[生理]表皮生长因子，[生理]上皮生长因子；上表皮生长因素

ectoderm epidermis───外胚层表皮

双语使用场景

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。

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。

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。

Conclusion: Incidence of epidermolysis bullosa type eruption ought to be observed. . .───结论：应用上述药品时应注意观察大疱性表皮松解型药疹的发生。

Conclusions The causes and clinical features of drug-induced bullosa epidermolysis are extremely complicated.───结论大疱性表皮松解型药疹病因、临床表现复杂；

Analysis characteristic and regularity of epidermolysis bullosa type eruption.───探讨大疱性表皮松解型药疹的发生特点及一般规律。

Methods: Electron microscopy and indirect immunofluorescence were performed on skin samples from 7 patients with epidermolysis bullosa.───方法：分析7个组织病理表现为表皮下疱的先天性大疱性表皮松解症患者的透射电镜和免疫荧光表现。

I have finally learned how to say, that I have a rare orphan genetic skin disorder named recessive dystrophic epidermolysis bullosa.───现在我终于学会解释自己的病了：这是一种罕见的遗传性皮肤病，叫隐性遗传营养不良型大疱性表皮松解症。

英语使用场景

I have finally learned how to say, that I have a rare orphan genetic skin disorder named recessive dystrophic epidermolysis bullosa.

Preclinical progress has been achieved in the treatment of wounds, epidermolysis bullosa and ichthyosis.

Objective To investigate the experience of the specialized nursing of toxic epidermolysis, improve specialized nursing care and accelerate patients get well soon.

Objective:To study molecule in basement membrane by electron microscopy and indirect immunofluorescence in patients with inherited epidermolysis bullosa.

Conclusion:Incidence of epidermolysis bullosa type eruption ought to be observed...

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.

Analysis characteristic and regularity of epidermolysis bullosa type eruption.

Objective:Analysis characteristic and regularity of epidermolysis bullosa type eruption.

Epidermolysis bullosa acquisita(EBA) is an autoimmune subepidermal bullous disease. This disease is rare in childhood.