Pregnancy in Marfan Syndrome – Two Case Reports

Detalhes bibliográficos
Autor(a) principal: Isidro Amaral, P
Data de Publicação: 2016
Outros Autores: Campos, A, Patrício, L
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.17/4154
Resumo: Marfan syndrome is a connective tissue disorder, autosomal dominant, which affects multiple organ systems, namely the cardiovascular, ocular and skeletal. Morbidity and mortality result primarily from aortic and cardiac complications including dilatation, dissection and rupture of the aorta. As a result, pregnancy in women with the Marfan syndrome has an increased risk. Main causes of complications are related with hemodynamic and hormonal modifications caused by pregnancy. The approach to pregnancy in patients with this syndrome is challenging and deserves special care. A multidisciplinary surveillance plan should be developed with support from cardiology, maternal fetal medicine, anesthesiology, genetics and pediatrics.
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spelling Pregnancy in Marfan Syndrome – Two Case ReportsGravidez na Síndrome de Marfan – dois casos clínicosMarfan SyndromePregnancyAortic dilatationMAC OBSMarfan syndrome is a connective tissue disorder, autosomal dominant, which affects multiple organ systems, namely the cardiovascular, ocular and skeletal. Morbidity and mortality result primarily from aortic and cardiac complications including dilatation, dissection and rupture of the aorta. As a result, pregnancy in women with the Marfan syndrome has an increased risk. Main causes of complications are related with hemodynamic and hormonal modifications caused by pregnancy. The approach to pregnancy in patients with this syndrome is challenging and deserves special care. A multidisciplinary surveillance plan should be developed with support from cardiology, maternal fetal medicine, anesthesiology, genetics and pediatrics.Federação das Sociedades Portuguesas de Obstetrícia e GinecologiaRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEIsidro Amaral, PCampos, APatrício, L2022-07-28T09:16:17Z20162016-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/4154porActa Obstet Ginecol Port 2016;10(1):74-77info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:45:35Zoai:repositorio.chlc.min-saude.pt:10400.17/4154Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:21:29.575283Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Pregnancy in Marfan Syndrome – Two Case Reports
Gravidez na Síndrome de Marfan – dois casos clínicos
title Pregnancy in Marfan Syndrome – Two Case Reports
spellingShingle Pregnancy in Marfan Syndrome – Two Case Reports
Isidro Amaral, P
Marfan Syndrome
Pregnancy
Aortic dilatation
MAC OBS
title_short Pregnancy in Marfan Syndrome – Two Case Reports
title_full Pregnancy in Marfan Syndrome – Two Case Reports
title_fullStr Pregnancy in Marfan Syndrome – Two Case Reports
title_full_unstemmed Pregnancy in Marfan Syndrome – Two Case Reports
title_sort Pregnancy in Marfan Syndrome – Two Case Reports
author Isidro Amaral, P
author_facet Isidro Amaral, P
Campos, A
Patrício, L
author_role author
author2 Campos, A
Patrício, L
author2_role author
author
dc.contributor.none.fl_str_mv Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE
dc.contributor.author.fl_str_mv Isidro Amaral, P
Campos, A
Patrício, L
dc.subject.por.fl_str_mv Marfan Syndrome
Pregnancy
Aortic dilatation
MAC OBS
topic Marfan Syndrome
Pregnancy
Aortic dilatation
MAC OBS
description Marfan syndrome is a connective tissue disorder, autosomal dominant, which affects multiple organ systems, namely the cardiovascular, ocular and skeletal. Morbidity and mortality result primarily from aortic and cardiac complications including dilatation, dissection and rupture of the aorta. As a result, pregnancy in women with the Marfan syndrome has an increased risk. Main causes of complications are related with hemodynamic and hormonal modifications caused by pregnancy. The approach to pregnancy in patients with this syndrome is challenging and deserves special care. A multidisciplinary surveillance plan should be developed with support from cardiology, maternal fetal medicine, anesthesiology, genetics and pediatrics.
publishDate 2016
dc.date.none.fl_str_mv 2016
2016-01-01T00:00:00Z
2022-07-28T09:16:17Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.17/4154
url http://hdl.handle.net/10400.17/4154
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Acta Obstet Ginecol Port 2016;10(1):74-77
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dc.publisher.none.fl_str_mv Federação das Sociedades Portuguesas de Obstetrícia e Ginecologia
publisher.none.fl_str_mv Federação das Sociedades Portuguesas de Obstetrícia e Ginecologia
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