Abstract
Objectives: Cholesteryl ester storage disease (CESD) is a rare autosomal recessive disease, due to deficiency of lysosomal acid lipase (LAL) resulting in lysosomal cholesteryl ester and triglyceride accumulation, in liver and macrophages throughout the body. CESD generally manifests with hepatomegaly and liver cytolysis, associated with combined hyperlipidemia.
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