Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis.

We have identified the molecular defect in two siblings presenting with classical clinical and biochemical features of Fish Eye disease (FED), including corneal opacities, HDL cholesterol < 10 mg/dl, normal plasma cholesteryl esters, and elevated triglycerides. In contrast to previously reported...

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Bibliographic Details
Main Authors:	Klein, H G, Santamarina-Fojo, S, Duverger, N, Clerc, M, Dumon, M F, Albers, J J, Marcovina, S, Brewer, H B
Format:	Artigo
Language:	Inglês
Published:	1993
Subjects:	Research Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC293635/ https://ncbi.nlm.nih.gov/pubmed/8326012
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Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis.

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