Hypobetalipoproteinemia, Familial, Apolipoprotein B


Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type

Apolipoprotein B Deficiencies

Apolipoprotein B Deficiency

Apolipoprotein B Deficiency Disease

Hypobetalipoproteinemia, Familial, Apo B

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.