Angioedema recorrente – caso clínico
Main Author: | |
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Publication Date: | 2014 |
Other Authors: | , , , , |
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. |
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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 |
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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 |
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FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
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RCAAP |
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RCAAP |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
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info@rcaap.pt |
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1833599210553868288 |