Cystic Fibrosis: What It Is, Causes, Symptoms, and Treatment
Cystic fibrosis is a significant genetic disease that affects various organ systems, primarily the lungs and digestive system. During this condition, the body produces thick and sticky mucus. Over time, the mucus accumulates in the lungs and pancreatic ducts, causing blockages. Individuals with this condition, which can have a life-threatening course, generally have a shorter lifespan compared to healthy individuals. Until about 60-70 years ago, patients with cystic fibrosis only lived up to elementary school age. However, thanks to recent developments, individuals with this condition can now live into their 30s, 40s, and even beyond. The prevalence of cystic fibrosis in the population is approximately 1 in 3,000, and since 75% of newly diagnosed individuals are under the age of 2, it is important to raise awareness. Before answering frequently asked questions such as "What causes cystic fibrosis?" and "How is cystic fibrosis diagnosed?", it is important to first answer the question, "What is cystic fibrosis?"