Brazilian guidelines for the diagnosis and treatment of hereditary angioedema
p. 1627-1636
| Autores: | , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2011 |
| País: | Brasil |
| Institución: | Universidade Federal da Bahia (UFBA) |
| Repositorio: | Repositório Institucional da UFBA |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.ufba.br:ri/18108 |
| Acceso en línea: | http://repositorio.ufba.br/ri/handle/ri/18108 |
| Access Level: | acceso abierto |
| Palabra clave: | Hereditary angioedema C1 inhibitor Asphyxia Acute surgical abdomen Guidelines Consensus |
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| dc.title.pt_BR.fl_str_mv |
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema |
| dc.title.alternative.pt_BR.fl_str_mv |
Clinics |
| title |
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema |
| spellingShingle |
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema Bianchi, Pedro Giavina Hereditary angioedema C1 inhibitor Asphyxia Acute surgical abdomen Guidelines Consensus |
| title_short |
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema |
| title_full |
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema |
| title_fullStr |
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema |
| title_full_unstemmed |
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema |
| title_sort |
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema |
| dc.creator.none.fl_str_mv |
Bianchi, Pedro Giavina França, Alfeu T. Grumach, Anete S. Motta, Abílio A. Fernandes, Fátima R. Campos, Régis de Albuquerque Valle, Solange O. Rosário, Nelson A. Solé, Dirceu Bianchi, Pedro Giavina França, Alfeu T. Grumach, Anete S. Motta, Abílio A. Fernandes, Fátima R. Campos, Régis de Albuquerque Valle, Solange O. Rosário, Nelson A. Solé, Dirceu |
| author |
Bianchi, Pedro Giavina |
| author_facet |
Bianchi, Pedro Giavina França, Alfeu T. Grumach, Anete S. Motta, Abílio A. Fernandes, Fátima R. Campos, Régis de Albuquerque Valle, Solange O. Rosário, Nelson A. Solé, Dirceu |
| author_role |
author |
| author2 |
França, Alfeu T. Grumach, Anete S. Motta, Abílio A. Fernandes, Fátima R. Campos, Régis de Albuquerque Valle, Solange O. Rosário, Nelson A. Solé, Dirceu |
| author2_role |
author author author author author author author author |
| dc.subject.por.fl_str_mv |
Hereditary angioedema C1 inhibitor Asphyxia Acute surgical abdomen Guidelines Consensus |
| topic |
Hereditary angioedema C1 inhibitor Asphyxia Acute surgical abdomen Guidelines Consensus |
| description |
p. 1627-1636 |
| publishDate |
2011 |
| dc.date.issued.fl_str_mv |
2011 |
| dc.date.accessioned.fl_str_mv |
2015-10-13T12:28:26Z |
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2015-10-13T12:28:26Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
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http://repositorio.ufba.br/ri/handle/ri/18108 |
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1807-5932, |
| dc.identifier.number.pt_BR.fl_str_mv |
v. 66, n. 9 |
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1807-5932, v. 66, n. 9 |
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http://repositorio.ufba.br/ri/handle/ri/18108 |
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eng |
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eng |
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info:eu-repo/semantics/openAccess |
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openAccess |
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Brasil |
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http://dx.doi.org/10.1590/S1807-59322011000900021 |
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reponame:Repositório Institucional da UFBA instname:Universidade Federal da Bahia (UFBA) instacron:UFBA |
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2015-10-13T12:28:26Z2015-10-13T12:28:26Z20111807-5932,http://repositorio.ufba.br/ri/handle/ri/18108v. 66, n. 9p. 1627-1636Hereditary 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 health professionals and is therefore an underdiagnosed disease. The causes of death from hereditary angioedema include laryngeal edema with asphyxia. The estimated mortality rate in patients in whom the disease goes undetected and who are therefore incorrectly treated is 25-40%. In addition to edema of the glottis, hereditary angioedema often results in edema of the gastrointestinal tract, which can be incapacitating. Patients with hereditary angioedema may undergo unnecessary surgical interventions because the digestive tract can be the primary or only organ system involved, thus mimicking acute surgical abdomen. It is estimated that patients with hereditary angioedema experience some degree of disability 20-100 days per year. The Experts in Clinical Immunology and Allergy of the "Associação Brasileira de Alergia e Imunopatologia -ASBAI" developed these guidelines for the diagnosis, therapy, and management of hereditary angioedema.Submitted by Edileide Reis (leyde-landy@hotmail.com) on 2014-02-19T13:43:29Z No. of bitstreams: 1 Regis A. Campos.pdf: 254414 bytes, checksum: db4489a3c989b1cb781cd78756cb885c (MD5)Approved for entry into archive by Flávia Ferreira (flaviaccf@yahoo.com.br) on 2015-10-13T12:28:26Z (GMT) No. of bitstreams: 1 Regis A. Campos.pdf: 254414 bytes, checksum: db4489a3c989b1cb781cd78756cb885c (MD5)Made available in DSpace on 2015-10-13T12:28:26Z (GMT). No. of bitstreams: 1 Regis A. Campos.pdf: 254414 bytes, checksum: db4489a3c989b1cb781cd78756cb885c (MD5) Previous issue date: 2011http://dx.doi.org/10.1590/S1807-59322011000900021reponame:Repositório Institucional da UFBAinstname:Universidade Federal da Bahia (UFBA)instacron:UFBAHereditary angioedemaC1 inhibitorAsphyxiaAcute surgical abdomenGuidelinesConsensusBrazilian guidelines for the diagnosis and treatment of hereditary angioedemaClinicsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleBrasilinfo:eu-repo/semantics/openAccessengBianchi, Pedro GiavinaFrança, Alfeu T.Grumach, Anete S.Motta, Abílio A.Fernandes, Fátima R.Campos, Régis de AlbuquerqueValle, Solange O.Rosário, Nelson A.Solé, DirceuBianchi, Pedro GiavinaFrança, Alfeu T.Grumach, Anete S.Motta, Abílio A.Fernandes, Fátima R.Campos, Régis de AlbuquerqueValle, Solange O.Rosário, Nelson A.Solé, DirceuORIGINALRegis A. Campos.pdfRegis A. 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