Comel‐Netherton syndrome: A local skin barrier defect in the absence of an underlying systemic immunodeficiency

BACKGROUND: Comel‐Netherton syndrome (NS) is a rare autosomal disease, characterized by severe skin disease, hair shaft defects, atopic diathesis, and increased susceptibility for skin infections. Since patients with NS suffer from recurrent infections, it has been hypothesized that an underlying im...

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Detalhes bibliográficos
Publicado no:Allergy
Main Authors: Stuvel, Kira, Heeringa, Jorn J., Dalm, Virgil A. S. H., Meijers, Ruud W. J., van Hoffen, Els, Gerritsen, Susan A. M., van Zelm, Menno C., Pasmans, Suzanne G. M. A.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
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ORIGINAL ARTICLES
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7384150/
https://ncbi.nlm.nih.gov/pubmed/31975472
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/all.14197
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