Introduction Cystic fibrosis (CF) is a hereditary disorder that primarily affects the lungs and digestive system. It is characterized by the production of abnormally thick and sticky mucus that can clog the airways and obstruct the pancreas. CF is a progressive disease, leading to severe respiratory and digestive problems, and it often results in a shortened lifespan. Causes Cystic fibrosis is caused by mutations in the CFTR (cystic fibrosis transmembrane conductance regulator) gene. This gene is responsible for the production of a protein that regulates the movement of salt and water in and out of cells. Mutations in the CFTR gene result in the production of a defective protein, leading to the accumulation of thick mucus in various organs. Symptoms The symptoms of cystic fibrosis can vary widely but commonly include: Respiratory symptoms: Persistent coughing, frequent lung infections (including pneumonia and bronchitis), wheezing, and shortness of breath. Digestive symptoms: Difficu...
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