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2.3.1.2 Anti-inflammatory effect of A1AT administration in cystic fibrosis Cystic fibrosis, a genetic disorder that primarily affects the lungs and digestive system, is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which leads to the production of defective CFTR proteins

Tac clearance is not affected by low-grade renal or liver dysfunction (83)

(each sachet contain 13.5 g.)

In pediatric care, targeted nutritional strategies should include individualized energy prescriptions based on growth velocity and developmental stage, systematic substitution of refined gluten-free staples with higher-fiber and higher-protein alternatives, and comprehensive micronutrient monitoring with supplementation as needed (94)