Cystic fibrosis is a genetic disorder that affects the lungs and digestive system, causing thick, sticky mucus to build up in the lungs and other organs. This leads to frequent lung infections, difficulty breathing, and poor growth and weight gain. Researchers are studying the underlying genetic mutations that cause cystic fibrosis, as well as looking for new treatments to help manage symptoms and improve quality of life for individuals with the condition. This research includes developing new medications, therapies, and approaches to improve lung function, decrease mucus production, and address other complications associated with cystic fibrosis. Additionally, researchers are exploring potential gene therapies and other innovative treatments to address the root cause of the disorder.