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

Lipid Disorders Main Page

Overview

Causes

Classification

Abetalipoproteinemia
Hypobetalipoproteinemia
Familial hypoalphalipoproteinemia
LCAT Deficiency
Chylomicron retention disease
Tangier disease
Familial combined hypolipidemia

Differential Diagnosis

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

Case Studies

Case#1


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