Cystic Fibrosis Essays -- essays research papers fc

Cystic Fibrosis is a severe hereditary disease that infects the lungs, digestive system, sweat glands and male fertility. The relieve oneself Cystic Fibrosis derives from the Fibrous scar tissue that develops in the pancreas. First recognised in 1938, cystic fibrosis is generalized as an autosomal recessive swage of the exocrine glands. About one in any 2500 Caucasians is affected, and one in 25 is a carrier of the cystic fibrosis gene. Cystic fibrosis is the most putting green fatal hereditary disorder of Caucasians in the United States and is the most public cause of chronic lung disease in children and preteen adults. Approximately 38,000 children and young adults in the United States today. About 3,000 babies are born with cystic fibrosis every year. Several decades ago many children with cystic fibrosis died by the age of 2. Today, active half of the people with cystic fibrosis live past the age of 31. That piece is expected to grow with the continuing success of modern treatment.Because cystic fibrosis is a genetic disease, it is caused by a defect in the psyche genes. These genes course of action the nucleus of all the bodys cells and control cell function, serving as the excogitation for the production of proteins (Gale 876). The defective gene that causes cystic fibrosis is called cystic fibrosis transmembrane conductance regulator, or for short, CFTR. It is the protein answerable for regulating chloride movement across cells in some tissues. When a person has two defective copies of the CFTR gene, cystic fibrosis is the result (Gale 876). There are over 500 known defects in the CFTR gene that can trigger cystic fibrosis (CF). The gene defects in cystic fibrosis are called point mutations. As a result, the CFTR protein made from the CFTR gene, is made incorrectly and cannot perform its function properly. The CFTR protein helps produce mucous secretion which is a mixture of salts, waters, sugars and proteins. The role of the CFTR protein is to allow chloride ions to exit the mucus producing cells. It helps to contain mucus from becoming to cryptic and sluggish, allowing the mucus to be moved steadily. In CF, the CFTR protein cannot do its job properly, and cannot allow chloride ions out of the mucus producing cells. The mucus becomes thick and can lead to malnutrition a... ...ng they might live to see the next day. BibliographyClaymen, Charles B. The American Medical Association Family Medical Guide. New York Random House., 1994Cotran, Ramzis S. Kumar, Vinay. Robbins, Stanley L. Pathologic substructure of Disease.Philadelphia, Pa WB Saunders Company., 1994Tierney, Lawerence M. Mcphee, Stephen J. Papadakis, Maxine A. Current Medical Diagnoisis and Treatment. Stamford, CT Appleton & Lange., 1997Gale, James. The Encyclopedia of catching Disorders and Birth Defects. New York Oxford., 1991Berhow, Robert. The Merck Manual of Medical Information. Whitehouse Station, NJ Merk & Co Inc., 1997