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abetalipoproteinemia

[ey-bey-tuh-lip-uh-proh-tee-nee-mee-uh, -tee-uh-nee-, -lahy-puh-, ey-bee-] /ˌeɪ beɪ təˌlɪp əˌproʊ tiˈni mi ə, -ti əˈni-, -ˌlaɪ pə-, ˌeɪ bi-/
noun, Pathology
1.
a rare inherited disorder of fat metabolism due to an inability to synthesize betalipoproteins necessary for the transport of triglycerides, leading to diarrhea, steatorrhea, and failure to thrive.
Origin
a-6 + betalipoprotein + -emia
Dictionary.com Unabridged
Based on the Random House Dictionary, © Random House, Inc. 2014.
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abetalipoproteinemia in Medicine

abetalipoproteinemia a·be·ta·lip·o·pro·tein·e·mi·a (ā-bā'tə-lĭp'ō-prō'tē-nē'mē-ə, -tē-ə-nē'-)
n.
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. Also called Bassen-Kornzweig syndrome.

The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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