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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Enregistré dans:
Détails bibliographiques
Auteurs principaux: Wahn, V., Aberer, W., Eberl, W., Faßhauer, M., Kühne, T., Kurnik, K., Magerl, M., Meyer-Olson, D., Martinez-Saguer, I., Späth, P., Staubach-Renz, P., Kreuz, W.
Format: Artigo
Langue:Inglês
Publié: Springer-Verlag 2012
Sujets:
Original Article
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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