Illness Cystic Fibrosis is a genetic disease that is passed down from both of the parents who have a copy of a defective in their DNA. There are variety of symptoms when it comes to cystic fibrosis such as: ‘Very salty-tasting skin‚ wheezing or shortness of breath‚ and male fertility ‘. There are no known cures for this genetic diseases‚ but there are treatments‚ and research that can help control this disease‚ and to possibly make a breakthrough discovery for a cure. I am patient who suffers from Cystic
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On researching new developments in the treatment of cystic fibrosis‚ I came across a very interesting article: “Ribosomal Stalk Protein Silencing Partially Corrects the ΔF508-CFTR Functional Expression Defect.” In the article‚ Viet et al1 reveal the potential application of the silencing of RPL12 (Ribosomal Protein L12)‚ to correct the ΔF508-CFTR biogenesis defect. As you know‚ cystic fibrosis is caused by a defect in the CF transmembrane conductance regulator (CFTR gene)‚ or more specifically‚ mutations
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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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as medical research has made substantial progress in recognizable disease today‚ there remains a plethora of diseases needed advanced research. Numerous diseases that were once an imminent death sentence have made outstanding medical advances. Cystic fibrosis (CF) is a genetic disorder that decreases the effectiveness of the lungs due to a mucous buildup. In the late twentieth century patients with CF could only to expect to live a few years but since 2006‚ life expectancy has risen to 36 years of
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is not growing at a normal rate. She has a persistent cough and foul smelling stool along with constipation. The only notable occurrence in her family history is a great-aunt who died of respiratory disease at 20 years old. Test results have shown high levels of sodium and chloride in her sweat. Patient A has Cystic Fibrosis‚ which is shown by her respiratory and digestive system symptoms. Cystic Fibrosis is a genetic mutation that mutates the cystic fibrosis transmembrane conductance regulator protein(CFTR)
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Cystic fibrosis‚ PKU and the Digestive system 1. What are the symptoms of cystic fibrosis and PKU with respect to the digestive system? Symptoms for cystic fibrosis include diarrhea that does not go away‚ foul-smelling stools‚ greasy stools‚ frequent urinating‚ frequent episodes of Pneumonia‚ persistent cough‚ skin tastes like salt‚ poor growth‚ chronic sinus infection. When phenylalanine builds up it affects brain functions and the central nervous system. Some symptoms include: skin problems
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FOCUS: “Treatments for lung conditions Cystic Fibrosis sufferers contend with” Word Count: 1461 This essay will aim to explore the different ideas and concepts of using several types of medication for cystic fibrosis sufferers. Cystic fibrosis is a genetic disorder that affects thousands of children and adults across the United Kingdom; it mainly affects Caucasian beings and is a well-known disease throughout the world‚ but has no cure only treatments to ensure a better quality of life
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Cystic Fibrosis is a life threatening condition that causes severe damage to the lungs and digestive system. Developing this condition can change a person’s entire life. Depending on the severity of the condition a person can be affected by mild symptoms such as shortness of breath‚ all the way to severe symptoms such as rectal prolapse‚ or even death. Screening is done on infants in all 50 states; therefore if a child has inherited Cystic Fibrosis it will be known in the first months of life. As
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Cystic fibrosis is a life – shortening inherited disorder that affects the way in which salt and water move into and out of the body’s cells. It effects mostly the lungs and the digestive system; where thick mucus blocks the small tubes and ducts of the pancreas. (Orenstein) The classic triad of exocrine abnormalities are pancreatic insufficiency‚ chronic recurrent pulmonary infections and an elevated sweat electrolyte concentration. At birth the pancreas shows signs of disease and the lungs appear
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Pulmonary fibrosis is the formation or development of excess fibrous connective tissue in the lungs. Pulmonary fibrosis is one of a family of related diseases called interstitial lung diseases. All of these diseases can result in lung scarring. (Ebina M 2010) "Fibrosis" is a term used to refer to scarring‚ so pulmonary fibrosis means scarring throughout the lungs. In some people‚ chronic pulmonary inflammation and fibrosis develop without an identifiable cause. Most of these people have a condition
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