Publication
A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge
dc.contributor.author | Mendes, C. | |
dc.contributor.author | Figueiredo, C. | |
dc.contributor.author | Mansilha, H. | |
dc.contributor.author | Proença, E. | |
dc.contributor.author | Oliveira, D. | |
dc.contributor.author | Lima, R. | |
dc.contributor.author | Carvalho, C. | |
dc.date.accessioned | 2015-10-27T10:47:24Z | |
dc.date.available | 2015-10-27T10:47:24Z | |
dc.date.issued | 2014-08-12 | |
dc.description.abstract | 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. | pt_PT |
dc.identifier | 10.4081/pr.2014.5596 | |
dc.identifier.citation | Pediatr Rep. 2014 ;6(3):5596 | pt_PT |
dc.identifier.doi | 10.4081/pr.2014.5596 | |
dc.identifier.issn | 2036-7503 | |
dc.identifier.uri | http://hdl.handle.net/10400.16/1869 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | PAGEPress | pt_PT |
dc.relation.publisherversion | http://www.pagepress.org/journals/index.php/pr/article/view/5596 | pt_PT |
dc.subject | microvillous inclusion disease | pt_PT |
dc.subject | protracted | pt_PT |
dc.subject | diarrhea | pt_PT |
dc.title | A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.conferencePlace | Italy | pt_PT |
oaire.citation.title | Pediatric reports | pt_PT |
oaire.citation.volume | 6(3) | pt_PT |
rcaap.rights | openAccess | pt_PT |
rcaap.type | article | pt_PT |