| Literature DB >> 22798447 |
Nafila Al Riyami1, Abdullah M Al-Ali, Ahmad J Al-Sarraf, John Hill, Kristina Sachs-Barrable, Robert Hegele, Kishor M Wasan, Jiri Frohlich.
Abstract
Hepatic lipase (HL) deficiency is a rare genetic disorder that has been associated with premature atherosclerosis despite high plasma high-density lipoprotein (HDL) cholesterol concentrations in the affected individuals. The authors describe the clinical and biochemical features of HL deficiency in a young male of Middle-Eastern-Arabic origin. This is the first report of cholesterol ester transfer protein (CETP) activity and mass in HL deficiency in a patient from this ethnic group. While the CETP mass was high, its activity was low, a discrepancy likely due to the abnormal composition of patient's HDL particles.Entities:
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Year: 2010 PMID: 22798447 PMCID: PMC3028409 DOI: 10.1136/bcr.12.2009.2589
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X