Primary hypoalphalipoproteinemia
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Familial hypoalphalipoproteinemia, FHA, familial HDL deficiency, FHD, high density lipoprotein deficiency, HDLD
Overview
Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner.[1]
It can be associated with LDL receptor.[2]
References
- ↑ Online Mendelian Inheritance in Man (OMIM) 604091
- ↑ Pisciotta L, Calabresi L, Lupattelli G; et al. (2005). "Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes". Atherosclerosis. 182 (1): 153–9. doi:10.1016/j.atherosclerosis.2005.01.048. PMID 16115486. Unknown parameter
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