Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/9433
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dc.contributor.authorÖzdemir, Özmert Muhammet Ali-
dc.contributor.authorÇıralı, Ceren-
dc.contributor.authorYılmaz Ağladıoğlu, Sebahat-
dc.contributor.authorEvrengül, Havva-
dc.contributor.authorTepeli, Emre-
dc.contributor.authorErgin, Hacer-
dc.date.accessioned2019-08-16T13:01:27Z-
dc.date.available2019-08-16T13:01:27Z-
dc.date.issued2016-
dc.identifier.issn1328-8067-
dc.identifier.urihttps://hdl.handle.net/11499/9433-
dc.identifier.urihttps://doi.org/10.1111/ped.12999-
dc.description.abstractNeonatal Bartter syndrome (NBS) is a rare autosomal recessive renal tubular disorder. This disease is characterized by hypokalemia, hypochloremia, and metabolic alkalosis that is often associated with failure to thrive and recurrent episodes of dehydration. The combination of BS and cholelithiasis in an infant is very rare. Herein, we report a premature male infant with NBS who developed cholelithiasis and hydrocephalus on clinical follow up. We recommend that periodic routine hepatobiliary ultrasonograpic screening for cholelithiasis should be performed in patients with NBS. © 2016 Japan Pediatric Societyen_US
dc.language.isoenen_US
dc.publisherBlackwell Publishingen_US
dc.relation.ispartofPediatrics Internationalen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectcholelithiasisen_US
dc.subjecthydrocephalusen_US
dc.subjectneonatal Bartter syndromeen_US
dc.subjectalanine aminotransferaseen_US
dc.subjectaspartate aminotransferaseen_US
dc.subjectbilirubinen_US
dc.subjectcholesterolen_US
dc.subjectgamma glutamyltransferaseen_US
dc.subjecthigh density lipoprotein cholesterolen_US
dc.subjectlow density lipoprotein cholesterolen_US
dc.subjectnitrogenen_US
dc.subjectsodium potassium chloride cotransporter 2en_US
dc.subjecttriacylglycerolen_US
dc.subjectureaen_US
dc.subjectadulten_US
dc.subjectApgar scoreen_US
dc.subjectartificial ventilationen_US
dc.subjectBartter syndromeen_US
dc.subjectcase reporten_US
dc.subjectclinical featureen_US
dc.subjectcomputer assisted tomographyen_US
dc.subjectdehydrationen_US
dc.subjectdisease associationen_US
dc.subjectechographyen_US
dc.subjectenteric feedingen_US
dc.subjectfetus distressen_US
dc.subjectfollow upen_US
dc.subjectgallstoneen_US
dc.subjectgeneen_US
dc.subjectgene mutationen_US
dc.subjecthumanen_US
dc.subjecthydramniosen_US
dc.subjecthypochloremiaen_US
dc.subjecthypokalemiaen_US
dc.subjectKCNJ1 geneen_US
dc.subjectkidney calcificationen_US
dc.subjectlaboratory testen_US
dc.subjectmaleen_US
dc.subjectmetabolic alkalosisen_US
dc.subjectNoteen_US
dc.subjectperinatal perioden_US
dc.subjectphysical examinationen_US
dc.subjectpolyuriaen_US
dc.subjectpremature laboren_US
dc.subjectpriority journalen_US
dc.subjectrare diseaseen_US
dc.subjectrespiratory distressen_US
dc.subjectSLC12A1 geneen_US
dc.subjectthorax radiographyen_US
dc.subjecttotal parenteral nutritionen_US
dc.subjecturea nitrogen blood levelen_US
dc.subjecturine volumeen_US
dc.subjectcomplicationen_US
dc.subjectfailure to thriveen_US
dc.subjectInfant, Premature, Diseasesen_US
dc.subjectnewbornen_US
dc.subjectprematurityen_US
dc.subjecttranscranial Doppler ultrasonographyen_US
dc.subjectx-ray computed tomographyen_US
dc.subjectBartter Syndromeen_US
dc.subjectCholelithiasisen_US
dc.subjectFailure to Thriveen_US
dc.subjectHumansen_US
dc.subjectHydrocephalusen_US
dc.subjectInfant, Newbornen_US
dc.subjectInfant, Prematureen_US
dc.subjectMaleen_US
dc.subjectTomography, X-Ray Computeden_US
dc.subjectUltrasonography, Doppler, Transcranialen_US
dc.titleNeonatal Bartter syndrome with cholelithiasis and hydrocephalus: Rare associationen_US
dc.typeNoteen_US
dc.identifier.volume58en_US
dc.identifier.issue9en_US
dc.identifier.startpage912-
dc.identifier.startpage912en_US
dc.identifier.endpage915en_US
dc.identifier.doi10.1111/ped.12999-
dc.relation.publicationcategoryDiğeren_US
dc.identifier.pmid27682612en_US
dc.identifier.scopus2-s2.0-84988935797en_US
dc.identifier.wosWOS:000387110700018en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale University-
item.openairetypeNote-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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