Doença de McArdle e Gravidez
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , |
Tipo de documento: | Relatório |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302019000100008 |
Resumo: | McArdle disease is a hereditary skeletal muscle disorder caused by myophosphorylase deficiency. This syndrome is characterized by exercise intolerance, fatigue, myalgias, cramps, and weakness. It is a rare disease, with few reported cases of pregnancy in women with this condition. Despite not having specific treatment, adequate physical activity can improve patient symptoms and prevent acute rhabdomyolysis. We present a case of a pregnant woman with McArdle disease. During pregnancy there was an improvement of exercise tolerance and creatine kinase levels. This case report illustrates our experience regarding the management of pregnancy and labour in women with McArdle disease. |
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Doença de McArdle e GravidezPregnancyMcArdleGlycogenMcArdle disease is a hereditary skeletal muscle disorder caused by myophosphorylase deficiency. This syndrome is characterized by exercise intolerance, fatigue, myalgias, cramps, and weakness. It is a rare disease, with few reported cases of pregnancy in women with this condition. Despite not having specific treatment, adequate physical activity can improve patient symptoms and prevent acute rhabdomyolysis. We present a case of a pregnant woman with McArdle disease. During pregnancy there was an improvement of exercise tolerance and creatine kinase levels. This case report illustrates our experience regarding the management of pregnancy and labour in women with McArdle disease.Euromédice, Edições Médicas Lda.2019-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/reporttext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302019000100008Acta Obstétrica e Ginecológica Portuguesa v.13 n.1 2019reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302019000100008Vilela,FernandaMartins,RitaEdral,AnaPacheco,Amáliainfo:eu-repo/semantics/openAccess2024-02-06T17:21:44Zoai:scielo:S1646-58302019000100008Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:28:40.482249Repositório 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 |
Doença de McArdle e Gravidez |
title |
Doença de McArdle e Gravidez |
spellingShingle |
Doença de McArdle e Gravidez Vilela,Fernanda Pregnancy McArdle Glycogen |
title_short |
Doença de McArdle e Gravidez |
title_full |
Doença de McArdle e Gravidez |
title_fullStr |
Doença de McArdle e Gravidez |
title_full_unstemmed |
Doença de McArdle e Gravidez |
title_sort |
Doença de McArdle e Gravidez |
author |
Vilela,Fernanda |
author_facet |
Vilela,Fernanda Martins,Rita Edral,Ana Pacheco,Amália |
author_role |
author |
author2 |
Martins,Rita Edral,Ana Pacheco,Amália |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Vilela,Fernanda Martins,Rita Edral,Ana Pacheco,Amália |
dc.subject.por.fl_str_mv |
Pregnancy McArdle Glycogen |
topic |
Pregnancy McArdle Glycogen |
description |
McArdle disease is a hereditary skeletal muscle disorder caused by myophosphorylase deficiency. This syndrome is characterized by exercise intolerance, fatigue, myalgias, cramps, and weakness. It is a rare disease, with few reported cases of pregnancy in women with this condition. Despite not having specific treatment, adequate physical activity can improve patient symptoms and prevent acute rhabdomyolysis. We present a case of a pregnant woman with McArdle disease. During pregnancy there was an improvement of exercise tolerance and creatine kinase levels. This case report illustrates our experience regarding the management of pregnancy and labour in women with McArdle disease. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-03-01 |
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=S1646-58302019000100008 |
url |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302019000100008 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S1646-58302019000100008 |
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 |
Euromédice, Edições Médicas Lda. |
publisher.none.fl_str_mv |
Euromédice, Edições Médicas Lda. |
dc.source.none.fl_str_mv |
Acta Obstétrica e Ginecológica Portuguesa v.13 n.1 2019 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799137356382470144 |