交界性大疱性表皮松解症(兽医)
大疱性表皮松解症
医学
皮肤病科
表皮(动物学)
病理
突变
遗传学
生物
解剖
基因
作者
Maximilian Kueckelhaus,Tobias Rothoeft,Laura De Rosa,Burcu Yeni,Tobias Ohmann,Christoph Maier,Lynn Eitner,Dieter Metze,Lorena Losi,Alessia Secone Seconetti,Michele De Luca,Tobias Hirsch
标识
DOI:10.1056/nejmoa2108544
摘要
Inherited junctional epidermolysis bullosa is a severe genetic skin disease that leads to epidermal loss caused by structural and mechanical fragility of the integuments. There is no established cure for junctional epidermolysis bullosa. We previously reported that genetically corrected autologous epidermal cultures regenerated almost an entire, fully functional epidermis on a child who had a devastating form of junctional epidermolysis bullosa. We now report long-term clinical outcomes in this patient. (Funded by POR FESR 2014-2020 - Regione Emilia-Romagna and others.).
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