1)epidermolysis bullosa simplex单纯性大疱性表皮松解症
1.Keratin gene mutation in a pedigree of Dowling-Meara epidermolysis bullosa simplex;Dowling-Meara型单纯性大疱性表皮松解症一家系角蛋白基因突变研究
2)epidermolysis bullosa大疱性表皮松解症
1.One Case Report of Epidermolysis Bullosa先天性大疱性表皮松解症1例
英文短句/例句
1.epidermolysis bullosa acquisita, EBA获得性大疱性表皮松解症
2.Laboratory Diagnoses of Epidermolysis Bullosa Acquisita;获得性大疱性表皮松解症的实验诊断
3.A case of recessive dystrophic epidermolysis bullosa隐性遗传营养不良型大疱性表皮松解症1例
4.Toxic bullosa epidermalysis associated with metamizole sodium tablets安乃近片相关中毒性大疱性表皮松解症
5.Dominant Dystrophic Epidermolysis Bullosa: Mutation Analysis;显性营养不良型大疱性表皮松解症的基因突变研究
6.The Report of One Clan with Dystrophic Epidermolysis Bullosa Dominant;遗传性营养不良型大疱性表皮松解症一家系报告
7.Treatment for dystrophic epidermolysis bullosa using tissue-engineering technique and cell therapy组织工程技术和细胞疗法治疗营养不良性大疱性表皮松解症
8.A family report of albopapuloid epidermolysis bullosa dystrophica dominant白色丘疹样显性营养不良型大疱性表皮松解症一家系报告
9.Mutation Analysis of COL7A1 Gene in Two Chinese Families with Dystrophic Epidermolysis Bullosa Pruriginosa;痒疹样营养不良型大疱性表皮松解症两家系基因突变分析
10.Family Survey of Clinicopathologic Characteristics of Dystrophic Epidermolysis Bullosa Pruriginosa痒疹样营养不良型大疱性表皮松解症两家系调查
11.A Recurrent Keratin 14 Mutation in Dowling-Mearaepidermolysis Bullosa Simplex单纯型大疱性表皮松解症Dowling-Meara亚型基因突变检测
12.Restoration of Recombinant Human Type VII Collagen and Correction of the Disease Phenotype in a Murine Model of Dystrophic Epidermolysis Bullosa;重组人VII型胶原蛋白对营养不良性大疱性表皮松解症治疗作用的实验研究
13.Dystrophic Epidermolysis Bullosa: Analysis of Clinical and Genetic Features and Study on the Structure Deficiency of Basement Membrane Zone;营养不良型大疱性表皮松解症：临床、遗传特点分析及其基底膜带结构缺陷的研究
14.hyperplastic epidermolysis bullosa增生性大疱性表皮松解
15.A Case of Epidermolysis Bullosa Drug Eruption Accompanied with Gastric Perforation大疱性表皮松解性药疹伴胃穿孔1例
16.Nursing of Bullous Epidermal Necrolysis Induced by Trichloroethylene三氯乙烯致大疱表皮坏死松解症的护理
17.Study on Gene Mutation of Two Dystrophic Epidermolysis Bullosa Pedigrees;两营养不良型大疱表皮松解症家系基因突变的研究
18.Nursing Care for A Patient with Severe Brain Injury Combined with Epidermolysis Bullosa1例重度颅脑损伤伴大疱性表皮松解型药疹患者的护理
相关短句/例句
epidermolysis bullosa大疱性表皮松解症
1.One Case Report of Epidermolysis Bullosa先天性大疱性表皮松解症1例
3)bullous epidermal necrolysis大疱性表皮坏死松解症
4)epidermolysis bullosa大疱性表皮松解
5)epidermolysis simplex单纯性表皮松解症
6)generalized atrophic benign epidermolysis bullosa泛发性萎缩性良性大疱性表皮松解症
1.Mutation analysis in one generalized atrophic benign epidermolysis bullosa family;泛发性萎缩性良性大疱性表皮松解症1例的基因突变研究
延伸阅读
获得性大疱性表皮松解症 以张力性大疱为基本损害的一种皮肤病。又名真皮松解性类天疱疮。1970年代后从先天性大疱性表皮松解症中分出来，并命名。特点是发病年龄多在40岁以上。尼科利斯基氏征阴性，皮疹好发于四肢远端。大疱的出现常以轻微外伤为诱因。愈后常留下瘢痕和粟丘疹。组织病理学检查为表皮下疱,疱内可见红细胞,疱下有嗜中性细胞为主的炎症细胞浸润。疱周皮肤直接免疫荧光检查显示基底膜带有线状 IgG沉积。免疫电镜则显示免疫球蛋白沉积于基底膜的致密板下带。本病的诊断标准为：①表皮下大疱；②无家族发病史；③病程慢性；④基底膜带线状IgG沉着,用1MNaCl分离正常人皮肤为底物,以间接免疫荧光法，可见荧光带在分离皮肤的真皮侧，这也是与大疱性类天疱疮主要鉴别点。本病无特效治疗方法，避免外伤为重要措施。皮疹较广泛者，必要时可应用皮质类固醇激素如泼尼松。预后良好。
