Cystic fibrosis is an inherited disease that ultimately leads to death. It affects every racial group worldwide, but its prevalence varies from country to country. In those with cystic fibrosis, the lungs and digestive system are primarily affected by the disease. With the new developments in treatment and management, the 50 percent survival rate from the 1970’s has greatly improved, allowing patients to continue to live their lives longer than ever expected in the past. The new developments in prevention of exacerbations, therapy drugs and methods to preserve lung function have done great things to help patients extend their lives. Education is another important aspect of treating cystic fibrosis. For example, more the patient knows about the disease and the benefits of the treatment, the more likely he, or she, is to comply with their recommended therapy. Though the treatment can be very costly and time consuming, it gives cystic fibrosis patients the opportunity to go to school, have jobs and even have families. These are normal events that go with aging that many cystic fibrosis patients may never have been able to dream of experiencing.
Cystic fibrosis is a recessive genetic disease. It is seen mainly in the Caucasian population, with 1 in 3,000 Caucasians having cystic fibrosis, but does affect every racial group. According to the Cystic Fibrosis Foundation Patient Registry, as of 2008, there were 30,000 patients with cystic fibrosis in the United States. Keeping this in mind, there are approximately 1,000 patients newly diagnosed with cystic fibrosis each year. The Cystic Fibrosis Foundation also estimates that there are approximately 70,000 children and adults with cystic fibrosis wo...
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...fibrosis. In (2011). A.D.A.M medical encyclopedia A.D.A.M., Inc. Retrieved from http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001167/
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Dowman, J. K., Watson, D., Loganathan, S., Gunson, B.K., Hodson, J., Mirza, D.F., Clarke, J., Lloyd C., Honeybourne D., Whitehouse, J.L., Nash, E.F., Kelly, D., van Mourik, I., Newsome, P.N.. (2012). Long-term impact of liver transplantation on respiratory function and nutritional status in children and adults with cystic fibrosis. American Journal of Transplantation,
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- Introduction Cystic fibrosis is an inherited disease that ultimately leads to death. It affects every racial group worldwide, but its prevalence varies from country to country. In those with cystic fibrosis, the lungs and digestive system are primarily affected by the disease. With the new developments in treatment and management, the 50 percent survival rate from the 1970’s has greatly improved, allowing patients to continue to live their lives longer than ever expected in the past. The new developments in prevention of exacerbations, therapy drugs and methods to preserve lung function have done great things to help patients extend their lives.... [tags: Diseases, Disorders]
1965 words (5.6 pages)
- The effects of cystic fibrosis can be broken down to a micro-perspective investigation in both the genotype, the encoding of the DNA, and the phenotype, the expression of DNA to trait. A precursor to the expression of cystic fibrosis, is through the inheritability pattern of cystic fibrosis from both parents. Cystic fibrosis is an autosomal recessive disease, meaning in the DNA of each parent, each had one copy of these recessive trait which is not expressed through them. However, with both parents being carriers, the offspring has a 25% chance of inheriting cystic fibrosis, a 25% chance of inheriting non-mutated genes and a 50% chance of being a carrier of the cystic fibrosis gene (Mayer-Ha... [tags: Mutation, DNA, Gene, Cystic fibrosis]
992 words (2.8 pages)
- Body imagine and disordered thoughts on eating among adolescents with Cystic Fibrosis Introduction: In order to orient the reader, the introduction will provide an overview of Cystic Fibrosis (CF) and eating disorders in the general population. This will then be followed by a consideration of both physiological and psychosocial aspects that may offer insight into factors that may make individuals with CF more vulnerable to developing disordered eating thoughts and behaviors in CF. Background to problem: Cystic Fibrosis (CF) is a life-threatening genetic disorder that is associated with respiratory and digestive problems and consequently inadequate nutrition and poor growth.... [tags: respiratory, body image, malnutrition]
2633 words (7.5 pages)
- Cystic Fibrosis Cystic Fibrosis is a genetic disease that affects many people today. It takes over a person’s whole life to survive this disease. To survive, people who suffer with Cystic Fibrosis need constant care of this disease. Cystic fibrosis is disorder that is inherited and causes severe damage to the lungs and digestive system. Cystic fibrosis changes the cells that make mucus, sweat and digestive juices. These fluids that are secreted are normally thin and slippery. A defective gene causes the secretions to become thick and sticky.... [tags: Cystic fibrosis, Genetics, Digestion, Pneumonia]
809 words (2.3 pages)
- Your child is under weight, has greasy, smelly diarrhea, a chronic cough and seems to always be getting pneumonia. He wheezes when he breathes and has impaired exercise ability. He seems to never being growing to the average size of his peers and his skin is very salty (5). The doctor’s first instinct should be to test your child for a disease called cystic fibrosis. Cystic fibrosis is a disease, which causes the mucus in your body to be thicker in some areas. The most affected areas are the lungs and digestive system.... [tags: Digestion, Cystic fibrosis, Pancreas, Cell]
1245 words (3.6 pages)
- Cystic Fibrosis Introduction Cystic fibrosis (CF) is an inherited chronic disease that must be carried by both parents in order to for the person to suffer from it. When two parents who are carriers have a child there is a 25 percent chance of having a child with CF and when one parents has CF and one parent is a carrier, there is a 50 percent chance of having a child with CF This disease affects organs such as the liver, lungs, pancreas, and intestines. This disease disrupts the body’s salt balance leaving too little salt and water on the outside of cells which makes the thin mucus that protects the linings of the airways, digestive system, reproductive system, and other organs and tissues... [tags: Cystic fibrosis, Pulmonology, Asthma]
1312 words (3.7 pages)
- Cystic fibrosis is a genetically inherited disease due to a mutation in the CFTR gene. This disease causes life changing health complications that affect many organs within the human body. There is always ongoing research for this disease to discover better treatment options that are more effective and possibly find a cure to reverse the mutated gene. The Cystic fibrosis transmembrane conductance regulator gene (CFTR) is responsible for providing the instructions to help make the protein that produces mucus in the body.... [tags: Cystic fibrosis, Genetics, Mutation, Asthma]
1836 words (5.2 pages)
- Cystic Fibrosis Cystic Fibrosis is a lung disease caused by a mutated gene. This gene called the CFTR gene causes a protein to not allow salt or water to flow through a cell properly. This produces a thick, sticky mucus to collect in the lungs and other organs. In order for a person to get this disease, the parents both have to be carriers of this disease. Usually a person is diagnosed within the first year of life. In the United States 1 in 2,500 to 3,500 Caucasian Americans, 1 in 17,000 African-Americans, and 31,000 Asian-Americans will have this disease.... [tags: Cystic fibrosis, Pulmonology, Asthma]
1397 words (4 pages)
- Overcoming Proteasomes: One Step Closer to a Cure for Cystic Fibrosis Take a deep breath and consider how easy it was to do so. Now picture struggling and gasping for air everyday; normal, easy tasks to the average person prove to be quite challenging to a patient of cystic fibrosis. Scientists have always been daunted by this fatal genetic disease that affects the body by excreting a “thick mucus” in the lungs, making breathing difficult and blocking the “ducts” leading from the pancreas, causing “poor digestion of food” (1).... [tags: Proteasomes Cystic Fibrosis]
1399 words (4 pages)
- Abstract: The main goal of this paper is to explain what Cystic Fibrosis is and also to explain what the causes of Cystic Fibrosis are. Cystic Fibrosis is caused by a mutation in a gene called Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). Cystic Fibrosis is known as one of the most common life-shortening disease. More that 1,000 mutations in the CFTR gene have been found in people with Cystic Fibrosis. Most of these mutations change single protein amino acids in the CFTR protein and it deletes a small amount of DNA from the CFTR gene.... [tags: Biology Medical CFTR Cystic Fibrosis]
717 words (2 pages)