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Our chosen charity is Cystic Fibrosis WA for which we have been raising funds since 1998. For more details on our past fundraising efforts see the Cystic Fibrosis page by clicking on the menu option to the left.
What is Cystic Fibrosis?
Cystic Fibrosis is a disorder in which the exocrine glands secrete abnormally thick mucus, leading to obstruction of the pancreas and chronic infections of the lungs, which generally cause death in childhood or early adulthood. Some mildly affected patients may survive longer. No cure for the disease has yet been found. Patients with pancreatic insufficiency can take pancreatic enzymes with meals. Those with respiratory infections are treated with antibiotics, with aerosols that relieve constriction of the airways, and by physical therapy to help them cough up the obstructing secretions. Intestinal obstruction, which occurs primarily in infancy (meconium ileus), may require surgery.
Cystic fibrosis is the most common inherited fatal disease of Caucasians, occurring about once in every 2500 births. Its occurrence in African-Americans is much lower-about one in every 17,000 births. If both parents carry the gene responsible for the disease, they have a one-in-four chance of having an affected child. In 1989, the gene responsible for cystic fibrosis was identified on chromosome 7. Since that time more than 200 different mutations in the cystic fibrosis gene have been described, and tests have been developed to detect the most common alterations. These tests can identify unaffected carriers of the disorder.
"Cystic Fibrosis," Microsoft(R) Encarta(R) 97 Encyclopedia. (c) 1993-1996 Microsoft Corporation. All rights reserved.
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