Angioedema recorrente – caso clínico

Bibliographic Details
Main Author: Martins, Sandrina
Publication Date: 2014
Other Authors: Salgado, Miguel, Raposo, Filipa, Pinto, Diana, Martinho, Isabel, Araújo, Rita
Format: Article
Language: por
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.16/1673
Summary: Introduction: Hereditary angioedema (HA) is a rare cause of recurrent angioedema caused by a default in the gene that encodes the C1 esterase inhibitor (C1-INH). The oedema involves predominantly the face, limbs and genital and gastrointestinal tract. The involvement of the larynx, although less frequent, is the most severe clinical expression of HA and is potentially fatal. Case report: Clinical report of an eight-year-old female with multiple episodes of angioedema. The laboratory study confirmed the diagnosis of HA. Discussion: HA diagnosis is established based on the clinical history, family history and complements testing. Its documentation is extremely important because it is potentially fatal and needs specific therapy.
id RCAP_ee35dcc6407463ee886e70559d543af0
oai_identifier_str oai:repositorio.chporto.pt:10400.16/1673
network_acronym_str RCAP
network_name_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository_id_str https://opendoar.ac.uk/repository/7160
spelling Angioedema recorrente – caso clínicoRecurrent angioedema – a case reportC1-INHchildrenhereditary angioedemarecurrenceAngioedema hereditáriocriançarecorrênciaIntroduction: Hereditary angioedema (HA) is a rare cause of recurrent angioedema caused by a default in the gene that encodes the C1 esterase inhibitor (C1-INH). The oedema involves predominantly the face, limbs and genital and gastrointestinal tract. The involvement of the larynx, although less frequent, is the most severe clinical expression of HA and is potentially fatal. Case report: Clinical report of an eight-year-old female with multiple episodes of angioedema. The laboratory study confirmed the diagnosis of HA. Discussion: HA diagnosis is established based on the clinical history, family history and complements testing. Its documentation is extremely important because it is potentially fatal and needs specific therapy.Nascer e CrescerRepositório Científico da Unidade Local de Saúde de Santo AntónioMartins, SandrinaSalgado, MiguelRaposo, FilipaPinto, DianaMartinho, IsabelAraújo, Rita2014-09-05T12:00:10Z2014-032014-03-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/1673por0872-0754info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-26T10:06:33Zoai:repositorio.chporto.pt:10400.16/1673Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T21:18:39.565052Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Angioedema recorrente – caso clínico
Recurrent angioedema – a case report
title Angioedema recorrente – caso clínico
spellingShingle Angioedema recorrente – caso clínico
Martins, Sandrina
C1-INH
children
hereditary angioedema
recurrence
Angioedema hereditário
criança
recorrência
title_short Angioedema recorrente – caso clínico
title_full Angioedema recorrente – caso clínico
title_fullStr Angioedema recorrente – caso clínico
title_full_unstemmed Angioedema recorrente – caso clínico
title_sort Angioedema recorrente – caso clínico
author Martins, Sandrina
author_facet Martins, Sandrina
Salgado, Miguel
Raposo, Filipa
Pinto, Diana
Martinho, Isabel
Araújo, Rita
author_role author
author2 Salgado, Miguel
Raposo, Filipa
Pinto, Diana
Martinho, Isabel
Araújo, Rita
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico da Unidade Local de Saúde de Santo António
dc.contributor.author.fl_str_mv Martins, Sandrina
Salgado, Miguel
Raposo, Filipa
Pinto, Diana
Martinho, Isabel
Araújo, Rita
dc.subject.por.fl_str_mv C1-INH
children
hereditary angioedema
recurrence
Angioedema hereditário
criança
recorrência
topic C1-INH
children
hereditary angioedema
recurrence
Angioedema hereditário
criança
recorrência
description Introduction: Hereditary angioedema (HA) is a rare cause of recurrent angioedema caused by a default in the gene that encodes the C1 esterase inhibitor (C1-INH). The oedema involves predominantly the face, limbs and genital and gastrointestinal tract. The involvement of the larynx, although less frequent, is the most severe clinical expression of HA and is potentially fatal. Case report: Clinical report of an eight-year-old female with multiple episodes of angioedema. The laboratory study confirmed the diagnosis of HA. Discussion: HA diagnosis is established based on the clinical history, family history and complements testing. Its documentation is extremely important because it is potentially fatal and needs specific therapy.
publishDate 2014
dc.date.none.fl_str_mv 2014-09-05T12:00:10Z
2014-03
2014-03-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.16/1673
url http://hdl.handle.net/10400.16/1673
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv 0872-0754
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Nascer e Crescer
publisher.none.fl_str_mv Nascer e Crescer
dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron:RCAAP
instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron_str RCAAP
institution RCAAP
reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
_version_ 1833599210553868288