Cholesterol ester storage disease: a reported case.

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dc.contributor.authorThavarungkul, Pen_US
dc.contributor.authorHemsrichart, Ven_US
dc.contributor.authorSupradish, Pen_US
dc.date.accessioned2009-05-27T19:24:18Z
dc.date.available2009-05-27T19:24:18Z
dc.date.issued1995-03-01en_US
dc.descriptionChotmaihet Thangphaet. 15 references.en_US
dc.description.abstractCholesterol ester storage disease is a rare autosomal recessive disease which is characterized by accumulation of cholesterol esters and triglycerides in the hepatocytes and other tissues. A 5-year and 4-month old Thai female with hepatosplenomegaly and hypercholesterolemia was diagnosed to have this disease by light and electron microscopic studies of the liver tissue from open biopsy. Early diagnosis and treatment with appropriate drug can help the patient by delaying the consequent complications. Genetic counselling and simplified explanation of the disease are a benefit to the patient's family.en_US
dc.description.affiliationInstitute of Pathology, Ministry of Public Health, Bangkok, Thailand.en_US
dc.identifier.citationThavarungkul P, Hemsrichart V, Supradish P. Cholesterol ester storage disease: a reported case. Journal of the Medical Association of Thailand. 1995 Mar; 78(3): 164-8en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/41061
dc.language.isoengen_US
dc.source.urihttps://www.mat.or.th/journal/all.phpen_US
dc.subject.meshBiopsy, Needleen_US
dc.subject.meshChild, Preschoolen_US
dc.subject.meshCholesterol Ester Storage Disease --diagnosisen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshMicroscopy, Electronen_US
dc.subject.meshThailanden_US
dc.titleCholesterol ester storage disease: a reported case.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
dc.typeReviewen_US
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