Publicação

Gravidez na Síndrome de Marfan: dois casos clínicos

Ver documento

Detalhes bibliográficos
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.
Autores principais:Amaral,Patrícia Isidro
Outros Autores:Campos,Ana; Patrício,Lino
Assunto:Marfan Syndrome Pregnancy Aortic dilatation
Ano:2016
País:Portugal
Tipo de documento:relatório
Tipo de acesso:acesso aberto
Instituição associada:Fundação para a Ciência e Tecnologia
Idioma:português
Origem:SciELO Portugal
_version_ 1868441862121979904
author Amaral,Patrícia Isidro
author2 Campos,Ana
Patrício,Lino
author2_role author
author
author_facet Amaral,Patrícia Isidro
Campos,Ana
Patrício,Lino
author_role author
country_str PT
creators_json_txt [{\"Person.name\":\"Amaral,Patrícia Isidro\"},{\"Person.name\":\"Campos,Ana\"},{\"Person.name\":\"Patrício,Lino\"}]
datacite.creators.creator.creatorName.fl_str_mv Amaral,Patrícia Isidro
Campos,Ana
Patrício,Lino
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Marfan Syndrome
Pregnancy
Aortic dilatation
datacite.titles.title.fl_str_mv Gravidez na Síndrome de Marfan: dois casos clínicos
dc.creator.none.fl_str_mv Amaral,Patrícia Isidro
Campos,Ana
Patrício,Lino
dc.format.none.fl_str_mv text/html
dc.identifier.none.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302016000100012
dc.language.none.fl_str_mv por
dc.publisher.none.fl_str_mv Euromédice, Edições Médicas Lda.
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.source.none.fl_str_mv Acta Obstétrica e Ginecológica Portuguesa v.10 n.1 2016
dc.subject.none.fl_str_mv Marfan Syndrome
Pregnancy
Aortic dilatation
dc.title.fl_str_mv Gravidez na Síndrome de Marfan: dois casos clínicos
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_93fc
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.
dirty 0
eu_rights_str_mv openAccess
format report
id scielopt_f7cd874dde94d5ecdc5baf2c09d9b8cb
identifier.url.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302016000100012
instacron_str SciELO
institution Fundação para a Ciência e Tecnologia
instname_str Fundação para a Ciência e Tecnologia
language por
network_acronym_str scielopt
network_name_str SciELO Portugal
oai_identifier_str oai:scielo:S1646-58302016000100012
organization_str_mv urn:organizationAcronym:scielo
person_str_mv Amaral,Patrícia Isidro
Campos,Ana
Patrício,Lino
publishDate 2016
publisher.none.fl_str_mv Euromédice, Edições Médicas Lda.
reponame_str SciELO Portugal
repository_id_str urn:repositoryAcronym:scielopt
service_str_mv urn:repositoryAcronym:scielopt
spelling Gravidez na Síndrome de Marfan: dois casos clínicosAmaral,Patrícia IsidroCampos,AnaPatrício,LinoMarfan SyndromePregnancyAortic dilatationopen accesshttp://purl.org/coar/access_right/c_abf2http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302016000100012URLhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302016000100012URLHasVersion2016-03-01Marfan 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.Euromédice, Edições Médicas Lda.Acta Obstétrica e Ginecológica Portuguesa v.10 n.1 2016text/htmlporreporthttp://purl.org/coar/resource_type/c_93fcother research product
spellingShingle Gravidez na Síndrome de Marfan: dois casos clínicos
Amaral,Patrícia Isidro
Marfan Syndrome
Pregnancy
Aortic dilatation
status SINGLETON
subject.fl_str_mv Marfan Syndrome
Pregnancy
Aortic dilatation
title Gravidez na Síndrome de Marfan: dois casos clínicos
title_full Gravidez na Síndrome de Marfan: dois casos clínicos
title_fullStr Gravidez na Síndrome de Marfan: dois casos clínicos
title_full_unstemmed Gravidez na Síndrome de Marfan: dois casos clínicos
title_short Gravidez na Síndrome de Marfan: dois casos clínicos
title_sort Gravidez na Síndrome de Marfan: dois casos clínicos
topic Marfan Syndrome
Pregnancy
Aortic dilatation
topic_facet Marfan Syndrome
Pregnancy
Aortic dilatation
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302016000100012
visible 1