交界性大疱性表皮松解症并发大疱性类天疱疮 - Suppr

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超能文献

Development of bullous pemphigoid in junctional epidermolysis bullosa.

作者信息

Fania L, Provini A, Salemme A, Sinagra J L, Guerra L, Mazzanti C, Didona B, Castiglia D, Di Zenzo G

机构信息

First Dermatologic Division, IDI-IRCCS, Rome, Italy.

Laboratory of Molecular and Cell Biology, IDI-IRCCS, Rome, Italy.

出版信息

J Eur Acad Dermatol Venereol. 2020 Mar;34(3):e146-e148. doi: 10.1111/jdv.16057. Epub 2020 Feb 13.

DOI:10.1111/jdv.16057

PMID:31709656

Abstract

摘要

相似文献

Development of bullous pemphigoid in junctional epidermolysis bullosa.交界性大疱性表皮松解症并发大疱性类天疱疮

J Eur Acad Dermatol Venereol. 2020 Mar;34(3):e146-e148. doi: 10.1111/jdv.16057. Epub 2020 Feb 13.

Bullous pemphigoid in a patient with suspected non-Herlitz junctional epidermolysis bullosa.疑似非 Haller-Junctional 型交界型大疱性表皮松解症患者的大疱性类天疱疮。

Clin Exp Dermatol. 2010 Dec;35(8):881-4. doi: 10.1111/j.1365-2230.2010.03828.x.

Generalized atrophic benign epidermolysis bullosa in 2 siblings complicated by multiple squamous cell carcinomas.2名兄弟姐妹患泛发性萎缩性良性大疱性表皮松解症，并发多发性鳞状细胞癌。

Arch Dermatol. 1998 Feb;134(2):199-203. doi: 10.1001/archderm.134.2.199.

Epidermolysis bullosa acquisita following bullous pemphigoid, successfully treated with the anti-CD20 monoclonal antibody rituximab.大疱性类天疱疮后获得性大疱性表皮松解症，用抗CD20单克隆抗体利妥昔单抗成功治疗。

Dermatology. 2007;215(3):252-5. doi: 10.1159/000106585.

Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations.通过框内跳跃含有无义或移码突变的外显子来减轻营养不良型和交界型大疱性表皮松解症的表型严重程度。

J Invest Dermatol. 1999 Sep;113(3):314-21. doi: 10.1046/j.1523-1747.1999.00709.x.

[Gene therapy for hereditary bullous epidermolysis].

Ann Dermatol Venereol. 2000 Mar;127(3):329-32.

[Gene therapy of junctional epidermolysis bullosa].

Med Sci (Paris). 2007 Jan;23(1):109-10. doi: 10.1051/medsci/2007231109.

E210K mutation in the gene encoding the beta3 chain of laminin-5 (LAMB3) is predictive of a phenotype of generalized atrophic benign epidermolysis bullosa.层粘连蛋白-5（LAMB3）β3链编码基因中的E210K突变可预测泛发性萎缩性良性大疱性表皮松解症的表型。

Br J Dermatol. 1998 Aug;139(2):325-31. doi: 10.1046/j.1365-2133.1998.02377.x.

Case of concurrent epidermolysis bullosa acquisita and anti-p200 pemphigoid--how to treat it?获得性大疱性表皮松解症与抗p200类天疱疮并发病例——如何治疗？

Int J Dermatol. 2007 Mar;46(3):295-8. doi: 10.1111/j.1365-4632.2006.02969.x.

Gene symbol: LAMB3. Disease: junctional epidermolysis bullosa, Herlitz variant.

Hum Genet. 2005 Dec;118(3-4):545.

引用本文的文献

Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening.病例报告：大疱性类天疱疮在营养不良型大疱性表皮松解症恶化的基础上发展。

Front Immunol. 2022 Jul 29;13:929286. doi: 10.3389/fimmu.2022.929286. eCollection 2022.

Occurrence of autoantibodies against skin proteins in patients with hereditary epidermolysis bullosa predisposes to development of autoimmune blistering disease.遗传性大疱性表皮松解症患者中针对皮肤蛋白的自身抗体的出现促使自身免疫性水疱病的发展。

Front Immunol. 2022 Jul 25;13:945176. doi: 10.3389/fimmu.2022.945176. eCollection 2022.

A Review of Acquired Autoimmune Blistering Diseases in Inherited Epidermolysis Bullosa: Implications for the Future of Gene Therapy.遗传性大疱性表皮松解症中获得性自身免疫性水疱病的综述：对基因治疗未来的启示

Antibodies (Basel). 2021 May 17;10(2):19. doi: 10.3390/antib10020019.

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