Duodenal atresia in neonatology: a case report (Atena Editora)

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MetadadosDescriçãoIdioma
Autor(es): dc.contributor.authorPEIXOTO, SINTHYA LORRANE ARAUJO-
Autor(es): dc.contributor.authorFARIAS, ANA RAQUEL ARAÚJO-
Autor(es): dc.contributor.authorFILHO, FRANCISCO TOMAZ DA COSTA-
Autor(es): dc.contributor.authorFILHO, ANTONIO HENRIQUE BARROSO DO VALE-
Autor(es): dc.contributor.authorNEGREIROS, MARIA TEREZA TEIXEIRA-
Autor(es): dc.contributor.authorQUEIROZ, SARAH CUNHA DE-
Data de aceite: dc.date.accessioned2023-10-05T14:07:26Z-
Data de disponibilização: dc.date.available2023-10-05T14:07:26Z-
Data de envio: dc.date.issued2023-10-02-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/738721-
Resumo: dc.description.abstractCongenital anomalies of the gastrointestinal tract occur when any portion of the gastrointestinal tract is affected, from the esophagus to the anus. Duodenal atresia is one of these manifestations, the third most common, and its incidence is estimated to be 1 in every 5,000 to 10,000 live births, affecting both sexes equally. It is characterized by failure to recanalize the duodenum after the seventh week of pregnancy and is correlated with genetic factors or some intrauterine ischemia. It causes intrinsic intestinal obstruction and can be detected by imaging through radiological topography, which highlights the characteristic finding of the disease (double gastric bubble), with the presence of air in the stomach and in the proximal stump of the duodenum, as seen in this case, in which it was evident gas distension in the topography of the newborn's epigastrium. It can be diagnosed in utero and has important repercussions on neonatal life, discussed in this work.pt_BR
Idioma: dc.language.isoenpt_BR
Palavras-chave: dc.subjectneonatologypt_BR
Título: dc.titleDuodenal atresia in neonatology: a case report (Atena Editora)pt_BR
Tipo de arquivo: dc.typelivro digitalpt_BR
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