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Metabolic Disorder

Hypobetalipoproteinemia, Familial, Apolipoprotein B

AMW:DIS:180045

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.

Pathology clinical

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