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Adult onset cystic fibrosis

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Beth Sercus, a year-old accounting consultant from Wharton, N. A resident she had never met walked into the hospital room and said, "We think your son might have cystic fibrosis. He may live to be 20 years old. You know, if he had cancer, he would have a better chance of survival.
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Older patients offer insight into the future of cystic fibrosis

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Cystic Fibrosis (Adults) | Michigan Medicine

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Cystic Fibrosis (Adults)

Cystic fibrosis CF is a genetic disorder that affects mostly the lungs , but also the pancreas , liver , kidneys , and intestine. CF is inherited in an autosomal recessive manner. There is no known cure for cystic fibrosis. CF is most common among people of Northern European ancestry and affects about one out of every 3, newborns. The main signs and symptoms of cystic fibrosis are salty-tasting skin , [11] poor growth, and poor weight gain despite normal food intake, [12] accumulation of thick, sticky mucus, [13] frequent chest infections, and coughing or shortness of breath.
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Jump to content. Cystic fibrosis is an inherited chronic disorder that causes mucus in the body to become thick and sticky. This glue-like mucus builds up and causes problems in many of the body's organs, especially the lungs, which can lead to infections, and the pancreas, making it difficult to properly digest food. 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.

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