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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
ORIGINAL ARTICLES
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384150/
https://www.ncbi.nlm.nih.gov/pubmed/31975472
http://dx.doi.org/10.1111/all.14197

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384150/
https://www.ncbi.nlm.nih.gov/pubmed/31975472
http://dx.doi.org/10.1111/all.14197

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