Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8117
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dc.contributor.authorErgin, H.-
dc.contributor.authorKüçüktasçi, K.-
dc.contributor.authorÖzdemir, O.M.A.-
dc.contributor.authorEliaçik, C.-
dc.contributor.authorGürses, Dolunay-
dc.contributor.authorYüksel, S.-
dc.contributor.authorPolat, A.-
dc.date.accessioned2019-08-16T12:35:40Z
dc.date.available2019-08-16T12:35:40Z
dc.date.issued2013-
dc.identifier.issn1300-0381-
dc.identifier.urihttps://hdl.handle.net/11499/8117-
dc.description.abstractA full term newborn having no underlying renal disease developed acute renal failure (ARF) after starting of oral enalapril (0.01mg/kg/day) given for the treatment of congestive heart failure (CHF). After peritoneal dialyses, she recovered from ARF. The patient treated due to yen tilatory associated pneumonia, sepsis and candidemia, developed left juguler venous thrombosis as sociated with central venous line by day 51 of life. Enoxaparine dose started 1.5 mg/kg/twice daily subcutaneously, was increased until reach recommended therapeutic target range of antifactor Xa. While she was treated with enoxaparine at a dose of 1.9 mg/kg/twice daily, thrombus propa gation was detected at her right juguler vein. Homozygote methylene tetrahydrofolatereductase (MTHFR) gene A1298C polymorphism was detected at the ethiology. Plasma homocysteine level and other prothrombotic components were normal. We suggest that, MTHFR gene A1298C poly morphism might be investigated in infants with ARF, venous thrombosis in spite of normal homo cysteine levels in the presence of prothrombotic risk factors such as CHF, sepsis, and catheter placement.. Copyright © 2013 by Türkiye Klinikleri.en_US
dc.language.isotren_US
dc.relation.ispartofTurkiye Klinikleri Pediatrien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcute renal injuryen_US
dc.subjectEnalaprilen_US
dc.subjectInfanten_US
dc.subjectMethylenetetrahydrofolate reductase (NADPH2)en_US
dc.subjectVenous thrombosisen_US
dc.subject5,10 methylenetetrahydrofolate reductase (FADH2)en_US
dc.subjectenalaprilen_US
dc.subjectenoxaparinen_US
dc.subjectacute kidney failureen_US
dc.subjectarticleen_US
dc.subjectcandidemiaen_US
dc.subjectcase reporten_US
dc.subjectcentral venous catheteren_US
dc.subjectcongestive heart failureen_US
dc.subjectDNA polymorphismen_US
dc.subjectenzyme polymorphismen_US
dc.subjectfemaleen_US
dc.subjecthomozygoteen_US
dc.subjecthumanen_US
dc.subjectjugular veinen_US
dc.subjectnewbornen_US
dc.subjectperitoneal dialysisen_US
dc.subjectsepsisen_US
dc.subjectvein thrombosisen_US
dc.subjectventilator associated pneumoniaen_US
dc.titleEnalapril-induced acute retal failure and jugular venous thrombosis associated with a homozygous methylene tetrahydrofolate reductase A1298C polymorphisms in a newborn with central venous line: Case reporten_US
dc.typeArticleen_US
dc.identifier.volume22en_US
dc.identifier.issue2en_US
dc.identifier.startpage90
dc.identifier.startpage90en_US
dc.identifier.endpage93en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-84877290811en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale University-
item.fulltextNo Fulltext-
item.languageiso639-1tr-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
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:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
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