Cystic fibrosis (CF) is an inherited autosomal recessive disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) protein.1 Over two thousand mutations have been identified, with F508del being the most common mutation.1 These mutations lead to multi-systematic disease involving pulmonary, gastrointestinal, reproductive, and endocrine systems.2 Here, CFTR is linked to cystic fibrosis.