Hereditary angioedema by C1 inhibitor-deficit: Diagnostic and therapeutic challenges. Case report
Background: Hereditary angioedema is a disease which manifests itself with episodes of spontaneous edema on skin, mucosal and airway. Treatment includes acute and prophylactic approach to minimize the attacks and severity. In many parts of the world, androgen derivatives, antifibrinolytic and fresh...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Colegio Mexicano de Inmunología Clínica y Alergia, A.C.
2017-12-01
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| Saila: | Revista Alergia México |
| Gaiak: | |
| Sarrera elektronikoa: | http://revistaalergia.mx/ojs/index.php/ram/article/view/310 |
| Etiketak: |
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