Cystic fibrosis (CF) is a genetic disorder that primarily affects the respiratory and digestive systems. It is characterized by the production of thick, sticky mucus that can clog the airways and trap bacteria, leading to repeated, severe lung infections. This mucus also obstructs the pancreas, preventing natural enzymes from aiding in food digestion. Symptoms often include persistent cough, frequent lung infections, and poor growth. Treatment is comprehensive, involving chest physiotherapy, medication to thin mucus and manage infections, nutritional support, and in some cases, lung transplantation. Advances in treatment have significantly extended the life expectancy of those with CF. Explore further by
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