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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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| 發表在: | Allergy |
|---|---|
| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2020
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| 主題: | |
| 在線閱讀: | 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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