Health condition · plain-language reference
Cystic Fibrosis
Also called: CF
Cystic fibrosis (CF) is an inherited disease of the mucus and sweat glands. It affects mostly your lungs, pancreas, liver, intestines, sinuses, and sex organs. CF causes your mucus to be thick and sticky. The mucus clogs the lungs, causing breathing problems and making it easy for bacteria to grow. This can lead to repeated lung infections and lung damage. The symptoms and severity of CF can vary. Some people have serious problems from birth. Others have a milder version of the disease that doesn't show up until they are teens or young adults. Sometimes you will have few symptoms, but later you may have more symptoms. CF is diagnosed through various tests, such as gene, blood, and sweat tests. There is no cure for CF, but treatments have improved greatly in recent years. In the past, most deaths from CF were in children and teenagers. Today, with improved treatments, some people who have CF are living into their forties, fifties, or older. Treatments may include chest physical therapy, nutritional and respiratory therapies , medicines, and exercise. NIH: National Heart, Lung, and Blood Institute
Plain-language summary from MedlinePlus (NIH/NLM) ↗. For informational purposes only — not medical advice.
Medications used for cystic fibrosis
Drugs whose FDA labeling names this condition among its indications — informational, not a recommendation.
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