A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge

Detalhes bibliográficos
Autor(a) principal: Mendes, C.
Data de Publicação: 2014
Outros Autores: Figueiredo, C., Mansilha, H., Proença, E., Oliveira, D., Lima, R., Carvalho, C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.16/1869
Resumo: Congenital diarrhea comprises a broad range of pathologies and often requires a thorough workup and immediate treatment. Although rare, microvillous inclusion disease (MVID) should be included in differential diagnosis of this presentation in the neonate. We report the case of a 36-week newborn who developed signs of severe dehydration and lethargy, requiring fluid resuscitation and total parenteral nutrition. MVID was diagnosed by recognition of profuse secretory diarrhea after an exhaustive etiological investigation, confirmed by DNA analysis.
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spelling A case of Protracted Diarrhea in a Newborn: a Diagnostic Challengemicrovillous inclusion diseaseprotracteddiarrheaCongenital diarrhea comprises a broad range of pathologies and often requires a thorough workup and immediate treatment. Although rare, microvillous inclusion disease (MVID) should be included in differential diagnosis of this presentation in the neonate. We report the case of a 36-week newborn who developed signs of severe dehydration and lethargy, requiring fluid resuscitation and total parenteral nutrition. MVID was diagnosed by recognition of profuse secretory diarrhea after an exhaustive etiological investigation, confirmed by DNA analysis.PAGEPressRepositório Científico do Centro Hospitalar Universitário de Santo AntónioMendes, C.Figueiredo, C.Mansilha, H.Proença, E.Oliveira, D.Lima, R.Carvalho, C.2015-10-27T10:47:24Z2014-08-122014-08-12T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/1869engPediatr Rep. 2014 ;6(3):55962036-750310.4081/pr.2014.5596info: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:RCAAP2023-10-20T10:57:55Zoai:repositorio.chporto.pt:10400.16/1869Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:38:11.603516Repositório 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 A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
title A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
spellingShingle A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
Mendes, C.
microvillous inclusion disease
protracted
diarrhea
title_short A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
title_full A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
title_fullStr A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
title_full_unstemmed A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
title_sort A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
author Mendes, C.
author_facet Mendes, C.
Figueiredo, C.
Mansilha, H.
Proença, E.
Oliveira, D.
Lima, R.
Carvalho, C.
author_role author
author2 Figueiredo, C.
Mansilha, H.
Proença, E.
Oliveira, D.
Lima, R.
Carvalho, C.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Centro Hospitalar Universitário de Santo António
dc.contributor.author.fl_str_mv Mendes, C.
Figueiredo, C.
Mansilha, H.
Proença, E.
Oliveira, D.
Lima, R.
Carvalho, C.
dc.subject.por.fl_str_mv microvillous inclusion disease
protracted
diarrhea
topic microvillous inclusion disease
protracted
diarrhea
description Congenital diarrhea comprises a broad range of pathologies and often requires a thorough workup and immediate treatment. Although rare, microvillous inclusion disease (MVID) should be included in differential diagnosis of this presentation in the neonate. We report the case of a 36-week newborn who developed signs of severe dehydration and lethargy, requiring fluid resuscitation and total parenteral nutrition. MVID was diagnosed by recognition of profuse secretory diarrhea after an exhaustive etiological investigation, confirmed by DNA analysis.
publishDate 2014
dc.date.none.fl_str_mv 2014-08-12
2014-08-12T00:00:00Z
2015-10-27T10:47:24Z
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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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.16/1869
url http://hdl.handle.net/10400.16/1869
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pediatr Rep. 2014 ;6(3):5596
2036-7503
10.4081/pr.2014.5596
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv PAGEPress
publisher.none.fl_str_mv PAGEPress
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