High density lipoprotein pathophysiology: Difference between revisions
Jump to navigation
Jump to search
Rim Halaby (talk | contribs) Created page with "__NOTOC__ {{High density lipoprotein}} {{PleaseHelp}} ==References== {{Reflist|2}} {{Lipopedia}} Category:Lipopedia Category:Lipid disorders Category:Cardiology..." |
Rim Halaby (talk | contribs) No edit summary |
||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{High density lipoprotein}} | {{High density lipoprotein}} | ||
{{ | {{CMG}} | ||
==Overview== | |||
Low [[HDL]] levels can be classified into primary and secondary. Hypoalphalipoproteinemia refers to primary lipoprotein disorders that lead to a low level of [[HDL]]. These include [[apolipoprotein 1 deficiency]], [[Tangier disease]], [[LCAT deficiency]] and primary [[hypoalphalipoproteinemia]]. In addition, low [[HDL]] can be secondary to other medical conditions. | |||
==References== | ==References== | ||
Revision as of 17:41, 17 September 2013
|
High Density Lipoprotein Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Clinical Trials |
|
Case Studies |
|
High density lipoprotein pathophysiology On the Web |
|
American Roentgen Ray Society Images of High density lipoprotein pathophysiology |
|
Risk calculators and risk factors for High density lipoprotein pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Low HDL levels can be classified into primary and secondary. Hypoalphalipoproteinemia refers to primary lipoprotein disorders that lead to a low level of HDL. These include apolipoprotein 1 deficiency, Tangier disease, LCAT deficiency and primary hypoalphalipoproteinemia. In addition, low HDL can be secondary to other medical conditions.