| 单词 | abetalipoproteinemia |
| 释义 | 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.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 abetalipoproteinemiaa-6 + beta + lipoprotein + -emia Words nearby abetalipoproteinemiaaberration, Aberystwyth, ab esse, abessive, abet, abetalipoproteinemia, abettor, ab extra, abeyance, abeyant, abfarad Dictionary.com UnabridgedBased on the Random House Unabridged Dictionary, © Random House, Inc. 2020 Medical definitions for abetalipoproteinemiaabetalipoproteinemia [ 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.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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