TURNER SYNDROME – AN UNUSUAL CAUSE FOR AORTIC DISSECTION

Bibliographic Details
Main Author: Augusto, Rita
Publication Date: 2021
Other Authors: Campos, Jacinta, Coelho, Andreia, Coelho, Nuno, Pinto, Evelise, Semião, Carolina, Ribeiro, João, Brandão, Daniel, Canedo, Alexandra
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://doi.org/10.48750/acv.306
Summary: 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 DISSECTIONSÍNDROME DE TURNER – UMA CAUSA INCOMUM DE DISSECÇÃO AÓRTICATurner SyndromeAortic DissectionX ChromosomeBicuspid Aortic ValveCoarctationSíndrome de TurnerDissecção AórticaCromossoma XVálvula aórtica bicúspideCoartaçãoTurner 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.O Síndrome de Turner (TS) é uma doença genética feminina cujos sinais cardinais são a existência de baixa estatura e de defeitos congénitos a nível cardiovascular. Patologias congenitas ou adquiridas do foro cardiovascular ocorrem com frequência no TS, sendo potencialmente graves e responsáveis por doenças como a dissecção aórtica em mulheres jovens. Neste contexto, os autores descrevem um caso de dissecção aórtica tipo A numa mulher jovem com TS, destacando a necessidade de investigação adicional nestas doentes para evitar um cenário aórtico catastrófico.Sociedade Portuguesa de Angiologia e Cirurgia Vascular2021-03-05T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.48750/acv.306oai:ojs.acvjournal.com:article/306Angiologia e Cirurgia Vascular; Vol. 16 No. 4 (2020): December; 322-326Angiologia e Cirurgia Vascular; Vol. 16 N.º 4 (2020): Dezembro; 322-3262183-00961646-706Xreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPenghttp://acvjournal.com/index.php/acv/article/view/306https://doi.org/10.48750/acv.306http://acvjournal.com/index.php/acv/article/view/306/223Copyright (c) 2021 Angiologia e Cirurgia Vascularinfo:eu-repo/semantics/openAccessAugusto, RitaCampos, JacintaCoelho, AndreiaCoelho, NunoPinto, EveliseSemião, CarolinaRibeiro, JoãoBrandão, DanielCanedo, Alexandra2022-05-23T15:10:09Zoai:ojs.acvjournal.com:article/306Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T10:00:13.420312Repositórios 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
SÍNDROME DE TURNER – UMA CAUSA INCOMUM DE DISSECÇÃO AÓRTICA
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
Síndrome de Turner
Dissecção Aórtica
Cromossoma X
Válvula aórtica bicúspide
Coartação
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
Síndrome de Turner
Dissecção Aórtica
Cromossoma X
Válvula aórtica bicúspide
Coartação
topic Turner Syndrome
Aortic Dissection
X Chromosome
Bicuspid Aortic Valve
Coarctation
Síndrome de Turner
Dissecção Aórtica
Cromossoma X
Válvula aórtica bicúspide
Coartação
description 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 2021
dc.date.none.fl_str_mv 2021-03-05T00:00:00Z
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 https://doi.org/10.48750/acv.306
oai:ojs.acvjournal.com:article/306
url https://doi.org/10.48750/acv.306
identifier_str_mv oai:ojs.acvjournal.com:article/306
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://acvjournal.com/index.php/acv/article/view/306
https://doi.org/10.48750/acv.306
http://acvjournal.com/index.php/acv/article/view/306/223
dc.rights.driver.fl_str_mv Copyright (c) 2021 Angiologia e Cirurgia Vascular
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2021 Angiologia e Cirurgia Vascular
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
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; Vol. 16 No. 4 (2020): December; 322-326
Angiologia e Cirurgia Vascular; Vol. 16 N.º 4 (2020): Dezembro; 322-326
2183-0096
1646-706X
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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