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Updated: Jun 17, 2026

A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
Skin manifestations in familial heterozygous hypercholesterolemia
Lucia Pietroleonardo1, Thomas Ruzicka
1Department of Dermatology, Ludwig Maximilian University of Munich, Klinik und Poliklinik fur Dermatologie und Allergologie, Frauenlobstrasse 9-11, 80337 Munich. Lucia. Pietroleonardo@med.uni-muenchen.de
Abstract:
Familial hypercholesterolemia, a form of primary hyperlipoproteinemia, is an autosomal dominant disorder characterized by an increase in serum LDL cholesterol concentrations. Multiple types of xanthomas occur, such as tendinous, tuberous, subperiosteal, and xanthelasma. Intertriginous xanthomas are rare, but if present are pathognomonic in this disorder. We report a patient with multiple xanthomas including the very rare intertriginous variety.
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