[ey-bey-tuh-lip-uh-proh-tee-nee-mee-uh, -tee-uh-nee-, -lahy-puh-, ey-bee-]
noun Pathology.
  1. a rare inherited disorder of fat metabolism due to an inability to synthesize certain apolipoproteins necessary for the transport of triglycerides, leading to diarrhea, steatorrhea, and failure to thrive.

Origin of abetalipoproteinemia

Dictionary.com Unabridged Based on the Random House Unabridged Dictionary, © Random House, Inc. 2018

abetalipoproteinemia in Medicine


[ā-bā′tə-lĭp′ō-prō′tē-nēmē-ə, -tē-ə-nē-]
  1. An inherited disorder characterized by the absence of low-density lipoproteins in the plasma, the presence of acanthocytes in the blood, retinal pigmentary degeneration, malabsorption of fats, and neuromuscular abnormalities.Bassen-Kornzweig syndrome
The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.