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Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening
Autoimmune response to cutaneous basement membrane components superimposed on a genetic skin fragility disease, hereditary epidermolysis bullosa (EB), has been described, but its effects on disease course remain unclear. We report a 69-year-old individual with congenital skin fragility and acral tra...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374178/ https://www.ncbi.nlm.nih.gov/pubmed/35967298 http://dx.doi.org/10.3389/fimmu.2022.929286 |