Research on cystic fibrosis

Cystic fibrosis is a genetic disorder that affects the lungs and digestive system, causing thick, sticky mucus to build up in these organs. This can lead to severe respiratory issues and nutritional problems. Research focuses on understanding the genetic mutations that cause cystic fibrosis, improving treatments, and developing gene therapies. New medications can help manage symptoms and improve quality of life. Advances in screening and early diagnosis are also crucial. Overall, ongoing research aims to enhance care for individuals with cystic fibrosis and move closer to a potential cure.