Cystic Fibrosis: MedlinePlus
Cystic Fibrosis
URL of this page: http://www.nlm.nih.gov/medlineplus/cysticfibrosis.html
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 problems such as repeated lung infections and lung damage.
The symptoms and severity of CF vary widely. 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.
Although there is no cure for CF, treatments have improved greatly in recent years. Until the 1980s, most deaths from CF occurred in children and teenagers. Today, with improved treatments, some people who have CF are living into their forties, fifties, or older.
NIH: National Heart, Lung, and Blood Institute
MEDICAL ENCYCLOPEDIA
National Institutes of Health
- The primary NIH organization for research on Cystic Fibrosis is the National Heart, Lung, and Blood Institute
08/01/2012 08:00 PM EDT
08/01/2012 08:00 PM EDT
Source: National Heart, Lung, and Blood Institute -
Related MedlinePlus Page: Cystic Fibrosis
Related MedlinePlus Page: Cystic Fibrosis
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