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 abetalipoproteinemia

Words nearby abetalipoproteinemia

Medical definitions for abetalipoproteinemia

abetalipoproteinemia
[ ā-bā′tə-lĭp′ō-prō′tē-nēmē-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