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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419830/
https://www.ncbi.nlm.nih.gov/pubmed/22543566
http://dx.doi.org/10.1007/s00431-012-1726-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419830/
https://www.ncbi.nlm.nih.gov/pubmed/22543566
http://dx.doi.org/10.1007/s00431-012-1726-4

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