Primary hypoalphalipoproteinemia: Difference between revisions

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#Redirect [[Low HDL]]
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{{SK}} 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.<ref>{{OMIM|604091}}</ref>
 
[[Image:autodominant.jpg|{{PAGENAME}} has an autosomal dominant pattern of [[inheritance]].]]
 
It can be associated with [[LDL receptor]].<ref name="pmid16115486">{{cite journal |author=Pisciotta L, Calabresi L, Lupattelli G, ''et al'' |title=Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes |journal=Atherosclerosis |volume=182 |issue=1 |pages=153–9 |year=2005 |month=September |pmid=16115486 |doi=10.1016/j.atherosclerosis.2005.01.048 |url=http://linkinghub.elsevier.com/retrieve/pii/S0021-9150(05)00117-6}}</ref>
 
==References==
{{reflist|2}}
 
{{Lipidemias}}
 
 
[[Category:Genetic disorders]]
 
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Latest revision as of 18:32, 17 September 2013

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