Chronic pancreatitis (CP) and acute recurrent pancreatitis (ARP) in paediatric populations are typically caused by anatomical variants, i.e., pancreatic divisum, choledochal malformations, genetic mutations in cystic fibrosis transmembrane conductance regulator (CFTR), Protein Serine type 1 (PRSS1), serine protease inhibitor kazal type 1 (SPINK 1), chymotrypsin C (CTRC) and carboxy Discussion at an HPB MDT meetingtidase 1 (CPA1) genes, infections, autoimmune causes and trauma [1,2]. Here, CFTR is linked to chronic pancreatitis.