Brazilian guidelines for the diagnosis and treatment of hereditary angioedema

Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple organ involvement. It is caused by a quantitative or functional deficiency of the C1 inhibitor, which is a member of the serine protease inhibitor family. Hereditary angioedema is unknown to many heal...

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Detalles Bibliográficos
Autores principales: Giavina-Bianchi, Pedro, França, Alfeu T., Grumach, Anete S., Motta, Abílio A., Fernandes, Fátima R., Campos, Regis A., Valle, Solange O., Rosário, Nelson A., Solé, Dirceu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2011
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164416/
https://www.ncbi.nlm.nih.gov/pubmed/22179171
http://dx.doi.org/10.1590/S1807-59322011000900021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164416/
https://www.ncbi.nlm.nih.gov/pubmed/22179171
http://dx.doi.org/10.1590/S1807-59322011000900021

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