Cystic Fibrosis Research Paper

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Cystic fibrosis is a complex disease and the types and severity of symptoms can differ widely from person to person. Many different factors, such as age of diagnosis, can affect an individual's health and the course of the disease. People with cystic fibrosis are at greater risk of getting lung infections because thick, sticky mucus builds up in their lungs, allowing germs to thrive and multiply. Lung infections, caused mostly by bacteria, are a serious and chronic problem for many people living with the disease. Minimizing contact with germs is a top concern for people with Cystic fibrosis. Newborns with intestinal obstruction typically require surgery, whereas adults with distal intestinal obstruction syndrome typically do not. Treatment
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Cystic Fibrosis Gary Mayberry Medical Terminology Prof. Gardner Perspective: Cystic Fibrous is an autosomal recessive genetic disorder that effects the body's human body's lungs, pancreas, liver, and intestines also known as mucoviscidosis mostly found in those with european ancestry. Cystic Fibrous targets the respiratory system and effects an person's lungs aggressively leaving them with short breath and difficulty breathing. Though this diesese affects the respiratory…

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History of Cystic Fibrosis While people have unquestionably kicked the bucket of CF for a great many years, the first clear references to the illness stretch out back just a couple of hundreds of years. European legends from the Middle Ages cautioned "trouble is the tyke who tastes salty from a kiss on the forehead, for he is reviled, and soon amazing". References have been found in therapeutic writings as right on time as 1595 that connected salty skin and harm to the pancreas with death in youth…

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In the United States “cystic fibrosis is the most common life-threatening genetic disease in the white population (Rosenstein, 2017). According to Rosenstein, 1 out of every 3,300 white births in the United States have cystic fibrosis (CF). There have been many improvements involving treatments that has increased the life expectancy resulting in many patients with CF becoming adults. There are both genetic and environmental risks associated with cystic fibrosis. It can be carried as an autosomal…

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Cystic fibrosis can also affect your pancreas with the buildup of mucus in the pancreas prevents digestive enzymes from reaching the rest of the digestive system. Because the enzymes can’t reach the digestive system, your body will have a hard time absorbing nutrients and proteins. Having an lack of nutrients can cause a slow gain of weight. This mean people Cystic fibrosis tend to be very skinny, no what how much food he or she eats. There are other symptoms for Cystic fibrosis along with the pancreas…

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Cystic fibrosis (CF) is a common but life-threatening disorder that can damage the digestive system and lungs. It is a chronic (long lasting) hereditary disease. Cystic fibrosis affects the cells that produce sweat, mucus, and digestive juices. The fluids then become thick and sticky and plug up the ducts, passageways, and tubes. Unfortunately, Cystic fibrosis is a genetic disorder that cannot be prevented. Many of us carry a CF gene and yet do not have the symptoms, why? This is because a person…

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