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| __NOTOC__
| | #Redirect [[Familial hypoalphalipoproteinemia]] |
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| {{SK}} Familial hypoalphalipoproteinemia, FHA, familial HDL deficiency, FHD, high density lipoprotein deficiency, HDLD
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| ==Overview==
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| Hypoalphalipoproteinemia is a [[high-density lipoprotein]] deficiency, inherited in an [[autosomal]] [[dominant]] manner.<ref>{{OMIM|604091}}</ref>
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| [[Image:autodominant.jpg|{{PAGENAME}} has an autosomal dominant pattern of [[inheritance]].]]
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| 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>
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| ==References==
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| {{reflist|2}}
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| {{Lipidemias}}
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| [[Category:Genetic disorders]]
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