Cystic Fibrosis
Cystic Fibrosis (CF) is a genetic disorder that affects the lungs and digestive system, most commonly diagnosed in children. It leads to the production of thick, sticky mucus that clogs airways, causing breathing difficulties and frequent lung infections. This mucus can also obstruct the pancreas, hindering proper digestion and nutrient absorption. CF requires ongoing medical care, including medications, airway clearance techniques, and proper nutrition, to manage symptoms and improve quality of life. Advances in treatment have significantly enhanced the outlook for children with CF, enabling many to lead healthier lives.
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Cystic fibrosis is a genetic disorder that affects the lungs and digestive system. It causes the body to produce thick, sticky mucus that clogs airways, leading to breathing difficulties and respiratory infections. This mucus also interferes with the pancreas, making it hard for the body to absorb nutrients. Symptoms often include persistent cough, frequent lung infections, and difficulty gaining weight. It is caused by mutations in a specific gene, and while there is no cure, treatments like physiotherapy, medications, and dietary changes can help manage symptoms and improve quality of life.