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

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dc.citation.volume73
dc.contributor.authorGiavina-Bianchi, Pedro
dc.contributor.authorArruda, Luisa Karla
dc.contributor.authorAun, Marcelo V.
dc.contributor.authorCampos, Regis A.
dc.contributor.authorChong-Neto, Herberto J.
dc.contributor.authorConstantino-Silva, Rosemeire N.
dc.contributor.authorFernandes, Fatima R.
dc.contributor.authorFerraro, Maria F.
dc.contributor.authorFerriani, Mariana P. L.
dc.contributor.authorFranca, Alfeu T.
dc.contributor.authorFusaro, Gustavo
dc.contributor.authorGarcia, Juliana F. B.
dc.contributor.authorKomninakis, Shirley
dc.contributor.authorMaia, Luana S. M.
dc.contributor.authorMansour, Eli
dc.contributor.authorMoreno, Adriana S.
dc.contributor.authorMotta, Antonio A.
dc.contributor.authorPesquero, Joao B. [UNIFESP]
dc.contributor.authorPortilho, Nathalia
dc.contributor.authorRosario, Nelson A.
dc.contributor.authorSerpa, Faradiba S.
dc.contributor.authorSole, Dirceu
dc.contributor.authorTakejima, Priscila
dc.contributor.authorToledo, Eliana
dc.contributor.authorValle, Solange O. R.
dc.contributor.authorVeronez, Camila L. [UNIFESP]
dc.contributor.authorGrumach, Anete S.
dc.coverageSao Paulo
dc.date.accessioned2020-07-08T13:09:57Z
dc.date.available2020-07-08T13:09:57Z
dc.date.issued2018
dc.description.abstractHereditary 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 mortality rate ranging from 25% to 40% due to asphyxiation by laryngeal angioedema. Intestinal angioedema is another important and incapacitating presentation that may be the main or only manifestation during an attack. In this article, a group of experts from the "Associacao Brasileira de Alergia e Imunologia (ASBAI)'' and the "Grupo de Estudos Brasileiro em Angioedema Hereditario (GEBRAEH)'' has updated the Brazilian guidelines for the diagnosis and treatment of hereditary angioedema.en
dc.description.affiliationUniv Sao Paulo, Fac Med, Hosp Clin HCFMUSP, Div Imunol Clin & Alergia, Sao Paulo, SP, Brazil
dc.description.affiliationUniv Sao Paulo, Fac Med Ribeirao Preto, Ribeirao Preto, SP, Brazil
dc.description.affiliationFac Med Bahia, Dept Med Interna & Suporte Diagnost, Salvador, BA, Brazil
dc.description.affiliationUniv Fed Parana, Dept Pediat, Curitiba, Parana, Brazil
dc.description.affiliationFac Med ABC, Imunol Clin, Santo Andre, SP, Brazil
dc.description.affiliationHosp Servidor Publ Estadual Francisco Morato Oliv, Sao Paulo, SP, Brazil
dc.description.affiliationUniv Fed Rio de Janeiro, Dept Med Interna, Div Imunol, Rio De Janeiro, RJ, Brazil
dc.description.affiliationUniv Fed Minas Gerais, Dept Pediat, Div Imunol Clin & Alergia, Belo Horizonte, MG, Brazil
dc.description.affiliationUniv Estadual Campinas, Fac Ciencias Med, Div Imunol Clin & Alergia, Dept Med Interna, Campinas, SP, Brazil
dc.description.affiliationUniv Fed Sao Paulo, Dept Biofis, Sao Paulo, SP, Brazil
dc.description.affiliationEscola Super Ciencias Santa Casa Misericordia Vit, Vitoria, ES, Brazil
dc.description.affiliationUniv Fed Sao Paulo, Div Alergia Imunol & Reumatol Clin, Dept Pediat, Sao Paulo, SP, Brazil
dc.description.affiliationFac Med Sao Jose do Rio Preto, Div Alergia & Imunol Clin, Sao Jose Do Rio Preto, SP, Brazil
dc.description.affiliationUnifespUniv Fed Sao Paulo, Dept Biofis, Sao Paulo, SP, Brazil
dc.description.sourceWeb of Science
dc.description.sponsorshipCSL Boehring
dc.description.sponsorshipShire
dc.format.extent-
dc.identifierhttp://dx.doi.org/10.6061/clinics/2018/e310
dc.identifier.citationClinics. Sao Paulo, v. 73, p. -, 2018.
dc.identifier.doi10.6061/clinics/2018/e310
dc.identifier.fileS1807-59322018000100303.pdf
dc.identifier.issn1807-5932
dc.identifier.scieloS1807-59322018000100303
dc.identifier.urihttps://repositorio.unifesp.br/handle/11600/54325
dc.identifier.wosWOS:000431328700002
dc.language.isoeng
dc.publisherHospital Clinicas, Univ Sao Paulo
dc.relation.ispartofClinics
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectHereditary Angioedemaen
dc.subjectAngioedemaen
dc.subjectC1 Inhibitor Deficiencyen
dc.subjectCoagulation Factor XII Mutationsen
dc.subjectManagementen
dc.subjectGuidelinesen
dc.titleBrazilian Guidelines for Hereditary Angioedema Management-2017 Update Part 1: Definition, Classification and Diagnosisen
dc.typeinfo:eu-repo/semantics/article
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