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 Research Paper

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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Cystic Fibrosis Research Paper

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Cystic Fibrosis Research Paper

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 Research Paper

Although unknown to many, Cystic Fibrosis is the common cause of many deaths. Cystic Fibrosis is known as Cystic Fibrosis TransmembraneConductance Regulator or in short, CFTR. The genetic disorder CFTR (ID:ENSG00000001626) affects the lungs, livers, intestines and pancreas which progresses the body to a congested mucus that clogs exocrine glands and causes infection. It's a recessive genetic disease which implies that an individual must have both copies of the mutated gene, from mom and dad, to occur…

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Cystic Fibrosis Research Paper

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Cystic Fibrosis Research Paper

problems. The association led to the discovery of Cystic Fibrosis, and the condition was given the name “Cystic Fibrosis of the Pancreas.” By definition, the term “cystic fibrosis” indicates damage to the tissues of the urinary bladder and gallbladder. People affected by Cystic Fibrosis do not look any different from other people. Because the effects of CF are mostly internal, there are no clear visual indicators that someone suffers from Cystic Fibrosis, but there are other ways to tell. Frequent coughing…

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