Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity

Background Dystrophic epidermolysis bullosa pruriginosa (DEB‐Pr) is a rare subtype of hereditary epidermolysis bullosa, with a poorly understood pathogenesis and no satisfactory treatment. Objectives To assess the clinical and biological features, genetic basis and therapeutic management, to better...

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Veröffentlicht in:	Journal of the European Academy of Dermatology and Venereology 2022-01, Vol.36 (1), p.133-143
Hauptverfasser:	Darbord, D., Hickman, G., Pironon, N., Barbieux, C., Bonnet‐des‐Claustres, M., Titeux, M., Miskinyte, S., Cordoliani, F., Vignon‐Pennamen, M.D., Amode, R., Hovnanian, A., Bourrat, E.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Aged Collagen Type VII - genetics Epidermolysis Bullosa Dystrophica - genetics Filaggrin Proteins - genetics Humans Middle Aged Mutation Phenotype Retrospective Studies
Online-Zugang:	Volltext
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