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Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies
Hereditary angioedema due to C1 inhibitor (C1 esterase inhibitor) deficiency (types I and II HAE-C1-INH) is a rare disease that usually presents during childhood or adolescence with intermittent episodes of potentially life-threatening angioedema. Diagnosis as early as possible is important to avoid...
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| Auteurs principaux: | , , , , , , , , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Springer-Verlag
2012
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3419830/ https://ncbi.nlm.nih.gov/pubmed/22543566 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00431-012-1726-4 |
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