Step 1: Type I hyperlipoproteinemia is caused by a deficiency of the enzyme lipoprotein lipase (or its cofactor apo C-II), which normally clears triglyceride-rich particles from blood.
Step 2: Because chylomicrons cannot be broken down, they accumulate, producing very high triglyceride levels. The hallmark is therefore elevated chylomicrons.
Step 3: The enzyme itself is deficient, so option d (elevated lipoprotein lipase) is wrong; LDL and HDL elevations are not the defining feature of this autosomal recessive disorder.
Step 4: Clinically it presents in infancy with colicky abdominal pain, failure to thrive, and eruptive xanthomas, and is managed by restricting dietary fat. The correct answer is elevated chylomicrons.