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abetalipoproteinemia

[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.



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Noah was 5 months old when she was diagnosed with abetalipoproteinemia, a genetic condition that keeps the body from absorbing fats and fat-soluble vitamins.

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