The Cystic Fibrosis Foundation describes Cystic Fibrosis as “a progressive‚ genetic disease that causes persistent lung infections and limits the ability to breathe over time” (www.cff.org). People with Cystic Fibrosis suffer from an increase of mucus buildup in the lungs‚ pancreas‚ and the liver; Cystic Fibrosis also affects the Nose and sinuses‚ as well as the sweat glands. The only way that CF is transmitted is by a Cystic Fibrosis positive carrier. When two positive carriers have a baby there
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Cystic Fibrosis is a genetic disorder that block some areas of the body with a mass of mucus. This disease is very common and affects one out of four people. It can only show when the offspring inherits two copies of the defective Cystic Fibrosis gene. The gene controls movement of water and salt‚ which causes the mucus. Although this disease does not sound threatening‚ the levels of dangers vary. There are treatments for this disease and this insures to some that they can live almost normally. Cystic
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Cystic Fibrosis: What is Cystic Fibrosis: Cystic fibrosis (CF) is a lifelong hereditary/genetic disorder‚ meaning the disease can be passed on from parent to child and can be inherited. CF is not contagious. Both parents must be either a carrier or suffer from CF for the disease to be passed on however carriers show no symptoms that a suffer does. CF affects the respiratory system; mainly the lungs and some parts of the digestive and reproductive systems including the pancreas‚ liver and the vas
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ASSIGNMENT TITLE: ESSAY ASSIGNMENT SUBTITLE: CYSTIC FIBROSIS COURSE CODE: BIOL 172 COURSE TITLE: STRUCTURE AND FUNCTION OF THE HUMAN BODY II CRN: 12495 SEMESTER: STUDENT NAME: STUDENT ID: PROGRAMME: BSC GENERAL NURSING DATE OF SUBMISSION: 27-11-2012 LECTURER’S NAME: JO ELLEN COLE Cystic fibrosis is an inherited gene caused by a defective gene‚ which affects tissues that produce mucous secretions. Cystic fibrosis affects organs like the lungs‚ the gastrointestinal
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Cystic fibrosis is a crippling disease that affects thousands of people worldwide. Cystic fibrosis is an inherited disease of the secretory glands that causes persistent lung infections and limits the ability to breathe over time. It causes cells to produce thick and sticky mucus‚ sweat‚ and digestive juices that block airways‚ ducts‚ and passageways. There is no cure‚ but there are ways to manage symptoms. According to the World Health Organization‚ the occurrence of cystic fibrosis varies across
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Cystic Fibrosis is a disease that causes mucus like substance to accumulate in the lungs‚ digestion track and various parts of the body. This is a disorder of the exocrine glands. Cystic Fibrosis is most common in children and young adults. This disease is usually not found in people over the age of forty years old because you are born with the disease and normally die young. This is a very harsh disease that makes it extremely hard to breathe. There are over one-thousand people diagnosed with Cystic
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fragile-x‚" 2008). Huntington’s Disease (HD) is an autosomal dominant pattern of inheritance. Males and females are equally likely to inherit the mutant gene. The change in the gene takes place when the gene is passed from parent to child. Nontraditional inheritance plays a role in the development of HD when symptoms appear at an earlier age with each generation. The mutant genes repeat more times than the usual number in normal copies of these genes. It is not clear what causes a trinucleotide repeat
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Cystic fibrosis: Overview and Implications Christopher Phillips‚ SN BTC Blackhawk Technical College Health Promotion 02/14/13 Cystic Fibrosis: Overview and Implications Cystic fibrosis (CF) is a worldwide autosomal recessive disorder genetically inherited that causes chronic progressive health alterations of the bodily systems (Lyczak et al‚ 2004‚ p. 194). Mutations in the cystic fibrosis transmembrane conductance regulator gene (CFTR)‚ located on the long arm of chromosome seven‚ results
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Introduction: Cystic fibrosis (CF) also known as mucoviscidosis is an inherited disease that causes the body to produce mucus that’s extremely thick and sticky. The mucus in people with CF is thicker than normal because CF affects cells in the epithelium‚ the layer of cells that lines the passages in the body’s organs. In a person who does not have CF‚ the epithelial cells produce a thin‚ watery mucus that acts like a lubricant and helps protect the body’s tissues. In a person with CF‚ however
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8-27-13 Genetics Cystic Fibrosis Cystic Fibrosis is one of the most widespread genetic disorders in the modern world. While only 30‚000 members of the American population is affected by the disease‚ millions of Americans are carriers of the disease; the difference between carriers and sufferers of the disease lies in the autosomal recessive nature of Cystic fibrosis. A truly documented history of Cystic fibrosis did not exist until well into the 1930s‚ although people did have an idea of what
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