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dc.contributor.authorAtugluzeybek, Cigdem
dc.contributor.authorAlhaj, Safa
dc.contributor.authorOnal, Hasan
dc.contributor.authorAltun, Gurkan
dc.date.accessioned2021-03-02T21:15:43Z
dc.date.available2021-03-02T21:15:43Z
dc.date.issued2007
dc.identifier.citationOnal H., Atugluzeybek C., Alhaj S., Altun G., "Encephalopathy in type I hyperlipidemia", INDIAN PEDIATRICS, cilt.44, sa.4, ss.306-308, 2007
dc.identifier.issn0019-6061
dc.identifier.othervv_1032021
dc.identifier.otherav_060b9683-625f-4a7d-a200-86891108eb45
dc.identifier.urihttp://hdl.handle.net/20.500.12627/9929
dc.description.abstractFamilial chylomicronemia syndrome is a group of rare genetic disorders characterized by deficient activity of an enzyme lipoprotein lipase or apo-protein C-II deficiency. In this paper we present an infant with massive hyperchylomicronemia and severe pancreatitis. Exchange transfusion for controlling hypertriglyceridemia and pancreatitis led to an increase in hyperviscosity which resulted in encephalopathy.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.titleEncephalopathy in type I hyperlipidemia
dc.typeMakale
dc.relation.journalINDIAN PEDIATRICS
dc.contributor.department, ,
dc.identifier.volume44
dc.identifier.issue4
dc.identifier.startpage306
dc.identifier.endpage308
dc.contributor.firstauthorID96876


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