Management of Netherton syndrome and hereditary angioedema with concurrent biologic therapy: a case report
Netherton syndrome (NS) is a rare autosomal recessive disorder caused by SPINK5 mutations, leading to impaired skin barrier function and severe atopic manifestations. Hereditary angioedema due to C1 inhibitor deficiency (HAE-C1-INH) is a rare autosomal dominant disorder characterised by recurrent br...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Open Exploration Publishing Inc.
2026-05-01
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| coleção: | Exploration of Asthma & Allergy |
| Assuntos: | |
| Acesso em linha: | https://www.explorationpub.com/uploads/Article/A1009125/1009125.pdf |
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