Deficiency of bile acids due to peroxisomal disorder
Peroxisomal disorders are a group of inherited metabolic diseases characterized by dysfunctional peroxisomes, cellular organelles essential for lipid metabolism, including bile acid synthesis. A deficiency in bile acids due to peroxisomal dysfunction disrupts cholesterol breakdown and fat digestion, leading to severe hepatic, neurological, and systemic consequences. This article explores the mechanisms of bile acid deficiency