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dc.contributor.authorYetgin, S.
dc.contributor.authorAytac, S.
dc.contributor.authorGurakan, F.
dc.contributor.authorYurdakok, M.
dc.date.accessioned2019-12-10T10:49:50Z
dc.date.available2019-12-10T10:49:50Z
dc.date.issued2007
dc.identifier.issn0743-8346
dc.identifier.urihttps://doi.org/10.1038/sj.jp.7211657
dc.identifier.urihttp://hdl.handle.net/11655/14272
dc.description.abstractNonimmune hydrops fetalis may occur as a result of different etiological conditions and in about one-third of cases no cause could be identified. Here, we report two cases of nonimmune hydrops fetalis associated with hereditary spherocytosis and hemophagocytic hystiocytosis. We think that babies with hydrops fetalis born of consanguineous parents should be examined for hereditary diseases, and that these rare causes should be taken into account in problematic cases.
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.isversionof10.1038/sj.jp.7211657
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectObstetrics & Gynecology
dc.subjectPediatrics
dc.titleNonimmune Hydrops Fetalis In Two Cases Of Consanguineous Parents And Associated With Hereditary Spherocytosis And Hemophagocytic Hystiocytosis
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalJournal Of Perinatology
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume27
dc.identifier.issue4
dc.identifier.startpage252
dc.identifier.endpage254
dc.description.indexWoS
dc.description.indexScopus


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