Cystic fibrosis is an inherited chronic disorder that causes mucus in the body to become thick and sticky. While cystic fibrosis is usually diagnosed in childhood, adults with no symptoms (or mild symptoms) during their youth can still be found to have the disease.
Cystic fibrosis diagnosed at age 45 based on symptoms of acute pancreatitis There are other case reports of adult-onset clinical disease presenting with.
Improvements in screening and treatments mean people with cystic fibrosis now may live into their mid- to late 30s, on average, and some are.
Adult-diagnosed cystic fibrosis patients generally have a milder form of the mutation, which is associated with severe, early-onset disease.
Late Diagnosis. While the majority of new cystic fibrosis (CF) diagnoses are detected very early in life via newborn screening (available in most provinces), there.