Turner Syndrome - an unusual cause for aortic dissection

Detalhes bibliográficos
Autor(a) principal: Augusto,Rita
Data de Publicação: 2020
Outros Autores: Campos,Jacinta, Coelho,Andreia, Coelho,Nuno, Pinto,Evelise, Semião,Carolina, Ribeiro,João, Brandão,Daniel, Canedo,Alexandra
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-706X2020000400322
Resumo: Abstract Turner syndrome (TS) is a disorder of female development with cardinal features of short stature and congenital cardiovascular defects. Congenital or acquired cardiological problems occur commonly in TS, being potentially progressive and responsible for severe complications, such as aortic dissection in young women. Accordingly, we describe a case of type A aortic dissection occurring in a woman with TS, highlighting the need to prioritize investigation in those patients to avoid a catastrophic aortic scenario.
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spelling Turner Syndrome - an unusual cause for aortic dissectionTurner SyndromeAortic DissectionX ChromosomeBicuspid Aortic ValveCoarctationAbstract Turner syndrome (TS) is a disorder of female development with cardinal features of short stature and congenital cardiovascular defects. Congenital or acquired cardiological problems occur commonly in TS, being potentially progressive and responsible for severe complications, such as aortic dissection in young women. Accordingly, we describe a case of type A aortic dissection occurring in a woman with TS, highlighting the need to prioritize investigation in those patients to avoid a catastrophic aortic scenario.Sociedade Portuguesa de Angiologia e Cirurgia Vascular2020-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/reporttext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-706X2020000400322Angiologia e Cirurgia Vascular v.16 n.4 2020reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-706X2020000400322Augusto,RitaCampos,JacintaCoelho,AndreiaCoelho,NunoPinto,EveliseSemião,CarolinaRibeiro,JoãoBrandão,DanielCanedo,Alexandrainfo:eu-repo/semantics/openAccess2024-02-06T17:23:00Zoai:scielo:S1646-706X2020000400322Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T13:10:22.745889Repositórios 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 Turner Syndrome - an unusual cause for aortic dissection
title Turner Syndrome - an unusual cause for aortic dissection
spellingShingle Turner Syndrome - an unusual cause for aortic dissection
Augusto,Rita
Turner Syndrome
Aortic Dissection
X Chromosome
Bicuspid Aortic Valve
Coarctation
title_short Turner Syndrome - an unusual cause for aortic dissection
title_full Turner Syndrome - an unusual cause for aortic dissection
title_fullStr Turner Syndrome - an unusual cause for aortic dissection
title_full_unstemmed Turner Syndrome - an unusual cause for aortic dissection
title_sort Turner Syndrome - an unusual cause for aortic dissection
author Augusto,Rita
author_facet Augusto,Rita
Campos,Jacinta
Coelho,Andreia
Coelho,Nuno
Pinto,Evelise
Semião,Carolina
Ribeiro,João
Brandão,Daniel
Canedo,Alexandra
author_role author
author2 Campos,Jacinta
Coelho,Andreia
Coelho,Nuno
Pinto,Evelise
Semião,Carolina
Ribeiro,João
Brandão,Daniel
Canedo,Alexandra
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Augusto,Rita
Campos,Jacinta
Coelho,Andreia
Coelho,Nuno
Pinto,Evelise
Semião,Carolina
Ribeiro,João
Brandão,Daniel
Canedo,Alexandra
dc.subject.por.fl_str_mv Turner Syndrome
Aortic Dissection
X Chromosome
Bicuspid Aortic Valve
Coarctation
topic Turner Syndrome
Aortic Dissection
X Chromosome
Bicuspid Aortic Valve
Coarctation
description Abstract Turner syndrome (TS) is a disorder of female development with cardinal features of short stature and congenital cardiovascular defects. Congenital or acquired cardiological problems occur commonly in TS, being potentially progressive and responsible for severe complications, such as aortic dissection in young women. Accordingly, we describe a case of type A aortic dissection occurring in a woman with TS, highlighting the need to prioritize investigation in those patients to avoid a catastrophic aortic scenario.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-706X2020000400322
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-706X2020000400322
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-706X2020000400322
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Angiologia e Cirurgia Vascular
publisher.none.fl_str_mv Sociedade Portuguesa de Angiologia e Cirurgia Vascular
dc.source.none.fl_str_mv Angiologia e Cirurgia Vascular v.16 n.4 2020
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
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