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LAL-D: A LIFE-THREATENING GENETIC DISEASE WITH ONGOING, PROGRESSIVE, MULTIORGAN DAMAGE LEADING TO PREMATURE DEATH1

In patients with Lysosomal Acid Lipase Deficiency (LAL-D), 
uncontrolled accumulation of cholesteryl esters (CEs) and triglycerides (TGs) leads to systemic complications1

LEARN TO DIAGNOSE LAL-D

Reference:   1. Bernstein DL, et al. J Hepatol. 2013;58:1230-43. doi:10.1016/j.jhep.2013.02.014.

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