Primary hypoalphalipoproteinemia: Difference between revisions

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Revision as of 17:51, 17 September 2013

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 |month= ignored (help)

Template:Lipidemias

Template:WikiDoc Sources

[1] Online Mendelian Inheritance in Man (OMIM) 604091

[pmid16115486-2] 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 |month= ignored (help)

[1]

[2]

@@ Line 1: / Line 1: @@
-{{Infobox_Disease |
+__NOTOC__
-  Name           = {{PAGENAME}} |
-  Image          = |
-  Caption        = |
-  DiseasesDB     = |
-  ICD10          = {{ICD10|E|78|6|e|70}} |
-  ICD9           = {{ICD9|272.5}} |
-  ICDO           = |
-  OMIM           = 604091 |
-  MedlinePlus    = |
-  eMedicineSubj  = med |
-  eMedicineTopic = 3368 |
-  MeshID         = D052456 |
-}}
 {{SI}}
 {{CMG}}
+{{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>
-'''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]].]]
-[[Image:autodominant.jpg|thumb|left|{{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>

Primary hypoalphalipoproteinemia: Difference between revisions

Revision as of 17:51, 17 September 2013

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