Cystic Fibrosis Research Paper

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Cystic Fibrosis: The Lungs’ Worst Enemy
Ayde Blanco, Noelia Ezquivel, Hannah Jiao, Elaine Proa
Texas A&M International University

Abstract
Cystic Fibrosis, a recessively genetic received disease, is a dangerous lung defect that occurs in almost 200,000 people each year. It is only inherited and works by damaging the lungs and the digestive system. It hazardously affects cells that create mucus, sweat, and digestive juices inside of your body. While these fluids are meant to act as a lubricant, cystic fibrosis causes these fluids to become thick and sticky, blocking up tubes, ducts, and passageways. Although unlikely, this disease affects a small handful of people in the United States, making small, everyday tasks difficult due …show more content…
Unfortunately, aside from personal lifestyle choices, genetics can play a role in how well your lungs do their overall job. Cystic Fibrosis, an accelerating, genetic disease that causes “persistent lung infections and limits the ability to breathe overtime” , is one of the few types of diseases that affects the overall health of the lungs. It is very important to be aware of these types of infections, as they are genetically inherited and affect almost 200,000 individuals every year (Davies, 2007, p …show more content…
It’s a disease that currently has treatments that can only help monitor and control its growth and development throughout the lifespan of the contracted individual. Cystic fibrosis is a disease that should have more research done to inform more efficiently its causes and effects in that human body and to help find a cure to prevent deaths or any severe

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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Cystic Fibrosis Research Paper

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

child’s chromosomes to result in a difference in the appearance or functions of their child. Cystic fibrosis is one of the most common recessive genetic diseases passed down to children. The problems it causes, the lifestyle of a patient who has it, and the probability of passing Cystic Fibrosis along to their offspring are all things a person will have to deal if inherited. The disease of Cystic Fibrosis is a genetic disorder which is passed through the egg of a women when a sperm is united with…

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Cystic Fibrosis Research Paper

Mucoviscidosis commonly known as Cystic Fibrosis which is usually shortened to CF is a genetic disorder that effects 70,000 people world wide. The disease affects the respiratory and digestive systems which include primarily the lung, the pancreas, the liver, the kidneys and the intestine. Cystic Fibrosis is caused by a defective gene that causes difficulty breathing, coughing up mucus and can be life threatening without constant medical care and attention from doctors. “Cystic fibrosis is the most common fatal…

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Cystic Fibrosis Research Paper

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 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

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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Cystic Fibrosis Research Paper

Cystic fibrosis was discovered in 1989, and on average a person suffering from cystic fibrosis has a life span of 25-30 years, this being 50 years less than the average human being. It is both a common and deadly genetic condition of the secretory glands that causes the body to produce excess amounts of thick mucus, causing multiple problems inside the human body. These problems include lung infections (commonly bronchitis and pneumonia), constricting breathing and blocking the pancreas which stops…

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Cystic Fibrosis Research Paper

Cystic Fibrosis Cystic fibrosis is a disorder genetically passed on. In order for a child to be born with this disorder, both parents must possess the recessive gene causing cystic fibrosis. A mutation on chromosome number 7 is the cause for cystic fibrosis. When the CFTR protein is defective, the epithelial cells fail to regulate chloride passing over cell membranes. This causes the mucus lining of the lungs to become hypertonic, making the normally thin layer of mucus thick, and sticky. Being…

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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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