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A case of idiopathic congenital neonatal cholestasis in a patient with down syndrome

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dc.contributor.authorHuh, T.-
dc.contributor.authorDo, H.J.-
dc.contributor.authorPark, J.S.-
dc.contributor.authorYeom, J.S.-
dc.contributor.authorPark, E.S.-
dc.contributor.authorSeo, J.H.-
dc.contributor.authorLim, J.Y.-
dc.contributor.authorPark, C.-H.-
dc.contributor.authorWoo, H.O.-
dc.contributor.authorYoun, H.-S.-
dc.date.accessioned2022-12-27T02:38:26Z-
dc.date.available2022-12-27T02:38:26Z-
dc.date.issued2012-
dc.identifier.issn2234-8646-
dc.identifier.issn2234-8840-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/23261-
dc.description.abstractDown syndrome is a rare cause of neonatal cholestasis. Neonatal cholestasis in a patient with Down syndrome is usually associated with severe liver diseases, such as neonatal hemochromatosis, myeloproliferative disorder and intrahepatic bile duct paucity. We experienced a case of idiopathic neonatal cholestasis in a patient with Down syndrome, which resolved spontaneously. ? 2014 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherKorean Society of Pediartic Gastroenterology, Hepatology and Nutrition-
dc.titleA case of idiopathic congenital neonatal cholestasis in a patient with down syndrome-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.5223/pghn.2012.15.2.117-
dc.identifier.scopusid2-s2.0-84951952848-
dc.identifier.bibliographicCitationPediatric Gastroenterology, Hepatology and Nutrition, v.15, no.2, pp 117 - 121-
dc.citation.titlePediatric Gastroenterology, Hepatology and Nutrition-
dc.citation.volume15-
dc.citation.number2-
dc.citation.startPage117-
dc.citation.endPage121-
dc.type.docTypeArticle-
dc.identifier.kciidART001672124-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordAuthorCholestasis-
dc.subject.keywordAuthorDown syndrome-
dc.subject.keywordAuthorNeonate-
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