Apolipoprotein B Familial Hypobetalipoproteinemia

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4 relevant articles (0 outcomes, 0 trials/studies) found for this Disease

Description: An autosomal dominant disorder of lipid metabolism. It is caused by mutations of APOLIPOPROTEINS B, main components of CHYLOMICRONS and BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include abnormally low LDL, normal triglyceride level, and dietary fat malabsorption.

Also Known As:

Hypobetalipoproteinemia, Familial, Apolipoprotein B; Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type; Apolipoprotein B Deficiency Disease; Hypobetalipoproteinemia, Familial, Apo B; Apolipoprotein B Deficiencies; Apolipoprotein B Deficiency

Disease Context: Research Results

Nutritional and Metabolic Diseases

Metabolic Diseases: 1264

Lipid Metabolism Disorders: 85

Dyslipidemias: 3798

Hypolipoproteinemias: 24

Hypobetalipoproteinemias: 162

Apolipoprotein B Familial Hypobetalipoproteinemia: 4

Related Diseases

1.	Fatty Liver
1 Diseases and 2 more articles analyzed in the Research Interface, order at left...

Experts

1.	Shah, S S: 1 article (02/2001)
2.	Desai, H G: 1 article (02/2001)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Apolipoprotein B Familial Hypobetalipoproteinemia:

1.	TransaminasesIBA 10/01/1997 - "We report an asymptomatic 26-year-old man with persistently raised transaminases, in whom the diagnosis of heterozygous (familial) apolipoprotein B deficiency was made on the basis of characteristic lipid profile." 02/01/2001 - "Fatty liver and elevated transaminases with heterozygous apolipoprotein B deficiency." 10/01/1997 - "Homozygous apolipoprotein B deficiency can present with fatty liver and raised levels of transaminases" Get all the results and reference details, order at left...
2.	LDL CholesterolIBA 01/01/2003 - "Heterozygous apolipoprotein B deficiency is an uncommon cause of transaminase elevation, as indicated by low levels of cholesterol and low density lipoprotein-cholesterol" Get all the results and reference details, order at left...
3.	CholesterolIBA 01/01/2003 - "Heterozygous apolipoprotein B deficiency is an uncommon cause of transaminase elevation, as indicated by low levels of cholesterol and low density lipoprotein-cholesterol" Get all the results and reference details, order at left...
4.	ApolipoproteinsIBA 02/28/1995 - "To examine the consequences of apolipoprotein B deficiency in mice, we used gene targeting in mouse embryonic stem cells to generate mice containing an insertional disruption of the 5' region of the apolipoprotein B gene" Get all the results and reference details, order at left...
4 Drugs and Important Bio-Agents and 4 more articles analyzed in the Research Interface, order at left...

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