CF affects multiple organ systems, including the respiratory, gastrointestinal, and reproductive systems, due to mutations in the gene encoding the CF transmembrane conductance regulator (CFTR) ion channel [7,9] Consequent to this genetic mutation, CFTR dysfunction results in abnormal transport of salt and water across epithelial cell membranes throughout the body, causing thickening of mucus secretions [7,9]. This evidence concerns the gene CFTR and cystic fibrosis.