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10 : 193203 Knapp MJ, Knopman DS, Solomon PR, Pendlebury WW, Davis CS, Gracon SI

Clinical Significance: Acyl Carnitine Translocase Deficiency Mutations in the SLC25A20 gene , which encodes Acyl Carnitine Translocase , lead to Carnitine-Acylcarnitine Translocase Deficiency (CACT Deficiency)

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This product contains the servings indicated when measured exactly by weight

Acting as a natural alternative to corticosteroids for inflammation control

DED is associated with an imbalance in Th17/Treg cells, leading to increased Th17 polarization and secretion of pro-inflammatory cytokines like IL-17, causing epithelial damage (Ratay et al., 2017)