Individuals with Abetalipoproteinemia experience failure to thrive, fat malabsorption, vitamin deficiencies, and severe developmental issues due to the absence of ApoB-containing particles.

“AA lipopro Mia a condition in which basically APO B containing particles do not exist there is a mutation in the microsomal triglyceride transfer protein resulting in deficiencies of apol proteins b48 and b00 which are in chylomicrons and vldl LL Etc respectively Now what are the symptoms failure to thrive stool fat fatty stool with loss of vitamins there frothy stools foul smelling stools protruding abdomen intellectual disability Developmental Coordination Disorder a taxia that is a gate disorder muscle weakness slurred speech scoliosis of course this is an extreme example of this but this is an extreme example of what happens when you don't have LDL or cholesterol respectively with a lipo prmia or Smith lemon opit syndrome in your body”