Hereditary Angioedema Caused By C1-Esterase Inhibitor Deficiency: A Literature-Based Analysis and Clinical Commentary on Prophylaxis Treatment Strategies

Hereditary angioedema (HAE) caused by C1-esterase inhibitor deficiency is an autosomal-dominant disease resulting from a mutation in the C1-inhibitor gene. HAE is characterized by recurrent attacks of intense, massive, localized subcutaneous edema involving the extremities, genitalia, face, or trunk...

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Detalles Bibliográficos
Autores principales: Gower, Richard G, Busse, Paula J, Aygören-Pürsün, Emel, Barakat, Amin J, Caballero, Teresa, Davis-Lorton, Mark, Farkas, Henriette, Hurewitz, David S, Jacobs, Joshua S, Johnston, Douglas T, Lumry, William, Maurer, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Allergy Organization 2011
Materias:
Supplement
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666183/
https://www.ncbi.nlm.nih.gov/pubmed/23283143
http://dx.doi.org/10.1097/1939-4551-4-S2-S9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666183/
https://www.ncbi.nlm.nih.gov/pubmed/23283143
http://dx.doi.org/10.1097/1939-4551-4-S2-S9

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