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Apolipoprotein B Familial Hypobetalipoproteinemia Summary

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 Show All >>

Key Drugs and Agents for Apolipoprotein B Familial Hypobetalipoproteinemia

Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
  1. Transaminases : 2 results : IBA
  2. LDL Cholesterol : 1 result : IBA
  3. Cholesterol : 1 result : IBA
  4. Apolipoproteins : 1 result : IBA

Diseases Related to Apolipoprotein B Familial Hypobetalipoproteinemia

  1. Fatty Liver

Key Therapies for Apolipoprotein B Familial Hypobetalipoproteinemia

Efficacy Chart >>

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