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Updated: Aug 31, 2025

A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
Case report: Unusual coexistence between familial hypercholesterolemia and familial hypobetalipoproteinemia
Kei Sasaki1,2, Hayato Tada3, Masa-Aki Kawashiri3
1Department of Internal Medicine, Self-Defense Forces Central Hospital, Tokyo, Japan.
Abstract:
Type 1 familial hypobetalipoproteinemia (FHBL1), characterized by low levels of apolipoprotein B (ApoB)-containing lipoproteins, elevation of transaminases, and hepatic steatosis, is a rare disease the prevalence of which is 1 in 3,000 among general population. Here we report an extremely rare family where phenotypes of familial hypercholesterolemia (FH) are canceled by coexistence of FHBL1 caused by an truncating mutation in apolipoprotein B (APOB).
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