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Updated: Jul 12, 2025

A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
Distinguishing Lysosomal Acid Lipase Deficiency From Familial Hypercholesterolemia
Sohum Sheth1, Peter P Toth2,3, Seth J Baum4,5
1University of Florida College of Medicine, Gainesville, Florida, USA.
Abstract:
Lysosomal acid lipase deficiency (LAL-D) is underrecognized because it manifests clinically with lipid and lipoprotein values similar to those observed in heterozygous familial hypercholesterolemia (FH). Although LAL-D is uncommon, understanding the differences between the 2 diseases has significant management implications. We present a case of LAL-D that masqueraded as FH. (Level of Difficulty: Advanced.).
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