Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis

Hereditary angioedema is an autosomal dominant disease characterized by recurrent angioedema attacks with the involvement of multiple organs. The disease is unknown to many health professionals and is therefore underdiagnosed. Patients who are not adequately diagnosed and treated have an estimated m...

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Hlavní autoři: Pedro Giavina-Bianchi, Luisa Karla Arruda, Marcelo V. Aun, Regis A. Campos, Herberto J. Chong-Neto, Rosemeire N. Constantino-Silva, Fátima R. Fernandes, Maria F. Ferraro, Mariana P.L. Ferriani, Alfeu T. França, Gustavo Fusaro, Juliana F.B. Garcia, Shirley Komninakis, Luana S.M. Maia, Eli Mansour, Adriana S. Moreno, Antonio A. Motta, João B. Pesquero, Nathalia Portilho, Nelson A. Rosário, Faradiba S. Serpa, Dirceu Solé, Priscila Takejima, Eliana Toledo, Solange O.R. Valle, Camila L. Veronez, Anete S. Grumach
Médium: Artigo
Jazyk:Inglês
Vydáno: Faculdade de Medicina / USP 2018-05-01
Edice:Clinics
Témata:
Hereditary Angioedema
Angioedema
C1 Inhibitor Deficiency
Coagulation Factor XII Mutations
Management, Guidelines
On-line přístup:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322018000100303&lng=en&tlng=en
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