Cystic fibrosis is an inherited disorder that affects the cells that produce mucus, sweat and digestive juices, leading to severe damage to the lungs and digestive system. These secreted fluids are normally thin and slippery. But in people with cystic fibrosis, a defective gene causes the secretions to become thick and sticky. Instead of acting as a lubricant, the secretions plug up tubes, ducts and passageways, especially in the lungs and pancreas.
These secreted fluids are normally thin and slippery. But in people with cystic fibrosis, a defective gene causes the secretions to become thick and sticky. Due to advances in screening and treatment people with cystic fibrosis are able to attend school and work and have a better quality of life than in previous decades.
Symptoms may worsen or improve as time passes. Some people may not experience symptoms until adolescence or adulthood.
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