Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency
Background: Hereditary angioedema (HAE) is a potentially life-threatening disorder characterized by recurrent episodes of subcutaneous or submucosal swelling. HAE with normal C1 inhibitor (HAE-nC1-INH) is an underdiagnosed condition. Although the association with genetic variants has been identified...
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| Autors principals: | , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2024-05-01
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| Col·lecció: | Journal of Allergy and Clinical Immunology: Global |
| Matèries: | |
| Accés en línia: | http://www.sciencedirect.com/science/article/pii/S2772829324000195 |
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