bullosa相关论文
BACKGROUND Dystrophic epidermolysis bullosa pruriginosa(DEB-Pr)is a rare subtype of DEB,characterized by recurrent pruri......
患者男,38岁.四肢反复起水疱、大疱伴痒38年,右踝部溃烂3年.小腿水疱处皮损组织病理示:表皮下水疱形成.直接免疫荧光:lgG、IgA、Ig......
近年来,随着分子遗传学研究的不断深入,越来越多的遗传性皮肤病致病基因得以明确,应用对致病基因的研究、载体构建、皮肤组织工程......
报道1例儿童获得性大疱性表皮松解症.患者女,12岁,因全身反复水疱、大疱和糜烂面3个月入院.患者弱智,父母非近亲结婚,无家族史.入......
报告1例常染色体隐性遗传的Hallopeau-Siemens型营养不良型大疱性表皮松解症.患者男,27岁.周身皮肤反复起水疱、破溃27年.患者出生......
报告1例大疱性蕈样肉芽肿。患者男，40岁。因躯干、四肢红斑伴瘙痒6年，出现斑块半年、水疱1个月就诊。皮肤科检查：面部、躯干及四肢泛......
Amyloidosis is characterized by extracellular deposition of abnormal protein, consisting of primary, secondary, hemodial......
Objective: The aim of the present study was to evaluate the structural variations of nasal cavity in reference to freque......
Fungal infection usually involves the paranasal sinuses. This is a rare case of fungal mass in concha bullosa. A 19-year......
Epidermolysis bullosa is a group of genetic disorderswith an autosomal dominant or an autosomal recessivemode of inherit......
Angina bullosa hemorrhagica(ABH)is an enigmatic oral disorder described for the first time by Badham in 1967 to define b......
目的：研究一营养不良型大疱表皮松解症家系的基因突变。方法：用组织病理，超微电镜及免疫荧光方法结合临床表现诊断为显性营养不良型大......
Epidermolysis Bullosa (EB) is a group of rare genetic skin conditions, which is characterised by extremely fragile skin ......
Summary:Non-Herlitz junctional epidermolysis bullosa(JEB-nH),an autosomal recessive bullous genodermatosis,is characteri......
报告1例痒疹样营养不良型大疱性表皮松解症，并进行了家系调查。先证者男，26岁。患者1岁左右时双踝部出现数个水疱，双胫前皮肤在外伤、......
