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A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
A case of homozygous familial hypercholesterolemia with an atypical phenotype and delayed clinical symptoms
Ondrej Kyselak1, Vladimir Soska1, Jan Kovar2
1Department of Clinical Biochemistry, St. Anne's University Hospital, Pekarska 53, 656 91 Brno, Czechia; Department of Laboratory Methods, Masaryk University, Komenskeho nam. 2, 602 00 Brno, Czechia.
Abstract:
We describe the casuistry of a homozygous familial hypercholesterolemia female patient with a biallelic missense variant (NM_000527.4:c.1775G>A, p.Gly592Glu) in the LDLR gene, severe hypertriglyceridemia and late manifestation of coronary heart disease not earlier than at the age of 45 years. An atypical phenotype led to a delayed diagnosis.
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