Cystic Fibrosis (CF) is a genetic disorder caused by mutations in the gene that encodes for the Cystic Fibrosis Transmembrane Regulator (CFTR) protein, an epithelial ion channel that is crucial in regulating the flow of negatively charged ions across membranes and ensuring adequate hydration of mucus as well as influencing immune responses in ways that are incompletely understood [1]. This evidence concerns the gene CFTR and cystic fibrosis.