Literature DB >> 6613682

Plasma lipid transfer in fish-eye disease.

G D Calvert, L A Carlson.   

Abstract

Fish-eye disease is a familial condition characterized by corneal opacities and dyslipoproteinaemia with, i.a., pronounced enrichment of plasma low density lipoprotein (LDL) with triglycerides. Cholesterol ester and triglyceride transferase activities in lipoprotein-free plasma have been measured in two patients with fish-eye disease and found to be normal. This indicates that a deficiency of plasma lipid transfer protein is not involved in the abnormal composition of LDL in fish-eye disease.

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Year:  1983        PMID: 6613682     DOI: 10.1111/j.0954-6820.1983.tb03729.x

Source DB:  PubMed          Journal:  Acta Med Scand        ISSN: 0001-6101


  4 in total

1.  Normalization of high density lipoprotein in fish eye disease plasma by purified normal human lecithin: cholesterol acyltransferase.

Authors:  L Holmquist; L A Carlson
Journal:  Lipids       Date:  1988-03       Impact factor: 1.880

2.  Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met).

Authors:  H G Klein; P Lohse; P H Pritchard; D Bojanovski; H Schmidt; H B Brewer
Journal:  J Clin Invest       Date:  1992-02       Impact factor: 14.808

Review 3.  Familial LCAT deficiency and fish-eye disease.

Authors:  N McIntyre
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

4.  Net lipid transfer between lipoproteins in fish-eye disease plasma supplemented with normal high density lipoproteins.

Authors:  L Holmquist; L A Carlson
Journal:  Lipids       Date:  1987-05       Impact factor: 1.880

  4 in total

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