Adult Cystic Fibrosis: Introduction. Adult Cystic Fibrosis: Cystic fibrosis is an inherited condition characterized by the production of thick sticky mucus by the mucus glands in the lungs, intestines, liver and pancreas. The condition is most often diagnosed in children or young adults but occasionally, relatively mild symptoms may lead to frequent misdiagnosis or no diagnosis at all unless Next: Symptoms of Adult Cystic Fibrosis. Cystic fibrosis is an inherited chronic disorder that causes mucus in the body to become thick and sticky. This glue-like mucus builds up and causes problems in many of the body's organs, especially the lungs, which can lead to infections, and the pancreas, making it difficult to properly digest food.
Cystic fibrosis is a genetic disorder affecting the digestive system and lungs. The disease affects cells producing digestive acids, sweat, and mucus. In healthy individuals, mucus is typically thin. However, individuals suffering from cystic fibrosis find their mucus sticky and thick. The role of mucus in the body is to provide lubrication for the airways, [ ]. What Are the Symptoms of Cystic Fibrosis? The symptoms of cystic fibrosis vary. Some children will have symptoms at birth, while others may not have symptoms for weeks, months, or even years.
Cystic fibrosis (CF) is a genetic disease that affects your lungs and other organs, too. This article explains what you can expect if you have it.