Hypolipoproteinemia: Difference between revisions
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==Classification== | ==Classification== | ||
Shown below is an algorithm depicting the classification of hypolipoproteinemia into primary and secondary. | |||
{{familytree/start |summary=Hypolipoproteinemia}} | |||
{{familytree | | | | | | | A01 | | | | | | | | A01= '''Hypolipoproteinemia'''}} | |||
{{familytree | |,|-|-|-|-|-|^|-|-|-|-|-|-|-|-|-|.| | | }} | |||
{{familytree | B01 | | | | | | | | | | | | | | B02 | B01= '''Primary'''<br>(Genetic)| B02= '''Secondary'''}} | |||
{{familytree | |!| | | | | | | | | | | | | | | |!| }} | |||
{{familytree | C01 | | | | | | | | | | | | | | C02 | C01=[[Abetalipoproteinemia]]<br> Apolipoprotein 1 deficiency <br> [[Chylomicron retention disease]] <br> Familial combined hypolipidemia <br> [[Hypobetalipoproteinemia]]<br> [[LCAT]] deficiency<br> Primary alphalipoproteinemia <br> [[PCSK9 deficiency]] <br> [[Tangier disease]]| C02= [[Anemia]] <br> [[Criticial illness]]<br> [[Chronic inflammation]] <br> [[Chronic liver disease]] <br> [[Hyperthyroidism]] <br>[[Infection]] <br> [[Malabsorption]] <br>[[Malignancy]]}} | |||
{{familytree/end}} | |||
==References== | ==References== |
Revision as of 21:47, 2 November 2016
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mohamed Moubarak, M.D. [2]
Synonyms and keywords: Hypolipidemia, low lipoprotein
Overview
Synopsis
Classification
Shown below is an algorithm depicting the classification of hypolipoproteinemia into primary and secondary.
Hypolipoproteinemia | |||||||||||||||||||||||||||||||||||||||||
Primary (Genetic) | Secondary | ||||||||||||||||||||||||||||||||||||||||
Abetalipoproteinemia Apolipoprotein 1 deficiency Chylomicron retention disease Familial combined hypolipidemia Hypobetalipoproteinemia LCAT deficiency Primary alphalipoproteinemia PCSK9 deficiency Tangier disease | Anemia Criticial illness Chronic inflammation Chronic liver disease Hyperthyroidism Infection Malabsorption Malignancy | ||||||||||||||||||||||||||||||||||||||||
References
Overview
Definition
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Hypolipoproteinemia from other Diseases
Epidemiology and Demographics
Risk Factors
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Future or Investigational Therapies