Statements in which the resource exists.
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pubmed-article:20052779pubmed:dateCreated2010-3-15lld:pubmed
pubmed-article:20052779pubmed:abstractTextWe report a Caucasian neonate with chronic non-spherocytic hemolytic anemia due to a class I G6PD deficiency. A novel mutation missense mutation in exon eight of the G6PD gene was detected (c.827C>T p.Pro276Leu). Bilirubin peaked on day 5 at 24 mg/dl with a conjugated bilirubin of 17 mg/dl. Jaundice resolved within 4 weeks. A detailed work-up failed to reveal other specific factors contributing to cholestasis. Severe hemolytic disease of the newborn may cause cholestasis even in the absence of associated primary hepato-biliary disease.lld:pubmed
pubmed-article:20052779pubmed:languageenglld:pubmed
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pubmed-article:20052779pubmed:monthMaylld:pubmed
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pubmed-article:20052779pubmed:authorpubmed-author:SchäferHansjö...lld:pubmed
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pubmed-article:20052779pubmed:authorpubmed-author:JankaGrittaGlld:pubmed
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pubmed-article:20052779pubmed:volume54lld:pubmed
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pubmed-article:20052779pubmed:year2010lld:pubmed
pubmed-article:20052779pubmed:articleTitleNeonatal cholestasis and glucose-6-P-dehydrogenase deficiency.lld:pubmed
pubmed-article:20052779pubmed:affiliationDepartment of Pediatric Hematology and Oncology, University Medical Center Eppendorf, Hamburg, Germany. kordes@uke.delld:pubmed
pubmed-article:20052779pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20052779pubmed:publicationTypeCase Reportslld:pubmed