Cholesteryl ester storage disease. Report of a case.

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T03:06:43Z
dc.date.accessioned2022-10-05T17:23:59Z
dc.date.available2014-05-27T03:06:43Z
dc.date.available2022-10-05T17:23:59Z
dc.date.created2014-05-27T03:06:43Z
dc.date.issued1987-07-01
dc.identifierArquivos de Gastroenterologia, v. 24, n. 3-4, p. 184-187, 1987.
dc.identifier0004-2803
dc.identifierhttp://hdl.handle.net/11449/63810
dc.identifier2-s2.0-0023379811
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3913985
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.
dc.languageeng
dc.relationArquivos de Gastroenterologia
dc.relation0,396
dc.rightsAcesso restrito
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.
dc.typeResenha


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