| abetalipoproteinaemia | <biochemistry, disease> A rare congenital disorder that causes the body to not produce chylomicrons, low density lipoprotein (LDL) and very low density lipoprotein (VLDL). Individuals with this condition are unable to properly digest fats. Other findings include ataxia, peripheral neuropathy and other forms of nerve dysfunction. Treatment includes vitamin E. Origin: Gr. Haima = blood (27 Sep 1997) |
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| normotriglyceridemic abetalipoproteinaemia | Abetalipoproteinaemia with normal levels of triglycerides. This inherited disorder (possibly autosomal recessive) is probably due to the absence of apolipoprotein B-100. (05 Mar 2000) |
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