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dc.contributor.authorCoelho, C. A.-
dc.contributor.authorBalarin, M. A.-
dc.contributor.authorCoelho, Kunie Iabuki Rabello-
dc.date.accessioned2014-05-27T03:06:43Z-
dc.date.accessioned2016-10-25T18:12:10Z-
dc.date.available2014-05-27T03:06:43Z-
dc.date.available2016-10-25T18:12:10Z-
dc.date.issued1987-07-01-
dc.identifier.citationArquivos de Gastroenterologia, v. 24, n. 3-4, p. 184-187, 1987.-
dc.identifier.issn0004-2803-
dc.identifier.urihttp://hdl.handle.net/11449/63810-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/63810-
dc.description.abstractCholesteryl ester storage disease (CESD) is a rare disorder of familial incidence characterized by the accumulation of cholesteryl ester and triglycerides in the liver, intestine and bone marrow. Until now only 21 cases have been reported in the literature. We present a 9 months old girl presenting with increased abdominal girth. She had normal liver function tests and increased cholesterol and triglycerides serum levels. The liver biopsy showed many cholesterol cristals seen as needle shaped cristals under polarized light. This is the youngest patient being diagnosed clinically in the literature.en
dc.format.extent184-187-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectcholesterol-
dc.subjecttriacylglycerol-
dc.subjectblood-
dc.subjectcase report-
dc.subjectcholesterol ester storage disease-
dc.subjectfemale-
dc.subjecthepatomegaly-
dc.subjecthuman-
dc.subjectinfant-
dc.subjectliver disease-
dc.subjectreview-
dc.subjectCase Report-
dc.subjectCholesterol-
dc.subjectCholesterol Ester Storage Disease-
dc.subjectFemale-
dc.subjectHepatomegaly-
dc.subjectHuman-
dc.subjectInfant-
dc.subjectLiver Diseases-
dc.subjectTriglycerides-
dc.titleCholesteryl ester storage disease. Report of a case.en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofArquivos de Gastroenterologia-
dc.identifier.scopus2-s2.0-0023379811-
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