Cystic fibrosis research paper outline. Sample Research Papers On Cystic Fibrosis 2022-10-26
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Cystic fibrosis (CF) is a chronic, genetic disease that affects the respiratory and digestive systems. It is caused by a mutation in the gene that encodes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein, which regulates the movement of salt and water in and out of cells. As a result of the mutation, thick and sticky mucus builds up in the lungs, pancreas, and other organs, leading to a range of serious health problems, including difficulty breathing, frequent lung infections, and malnutrition.
CF is a rare disease, affecting about 30,000 people in the United States and 70,000 people worldwide. It is most common in people of Northern European ancestry, but it can affect people of any racial or ethnic background. There is currently no cure for CF, but treatments such as antibiotics, airway clearance techniques, and nutritional support can help improve quality of life and extend lifespan.
Other complications (liver disease, diabetes, infertility)
III. Diagnosis and treatment of CF
Tests and procedures used to diagnose CF (sweat test, genetic testing)
Current treatments for CF (antibiotics, airway clearance techniques, nutritional support)
Experimental treatments and potential therapies (gene therapy, CFTR modulators)
IV. The impact of CF on patients and their families
Physical and emotional challenges of living with CF
Support systems for individuals with CF and their families
Advocacy and research efforts to find a cure for CF
Recap of the main points of the essay
Reflection on the importance of ongoing research and treatment for CF
Call to action for readers to learn more about CF and support efforts to find a cure.
Current and Future Cystic Fibrosis Research
About Cystic Fibrosis Marshall Influenza Case Study 728 Words 3 Pages Because they also encourage mucous secretions, macrophage activity on pneumococci is decreased while bacterial adhesion to the epithelium is increased. Consequently, such children have poor growth and development and experience reduced weight. The third goal is to manage any associated complication. Cystic Fibrosis Case Study 407 Words 2 Pages Maintaining a high level of exercise and fitness is basic for people living with cystic fibrosis. Research has shown that the formation of thick yet sticky mucus is associated to pancreatic dis- functioning because the digestive enzymes block the pancreatic duct, causing some limitations in the production of insulin. Hopefully, as the years go on and medical treatments improve with research and technology the rates of success for patients with this disorder will go up even more.
Cystic Fibrosis patients either produce uncommon CFTR protein or no CFTR protein at all. This kind of test helps in preventing symptoms before they appear. Just 50 years ago, no treatments for cystic fibrosis CF existed. One can predict the chances of the phenotype inheriting the cystic fibrosis gene from the genotype. The genes are so similar that people could argue that Judaism is a race. Oxford: Oxford University Press, 1995.
How do you prevent your child from having cystic fibrosis you may ask? There is another aspect of the treatment that is noted to be essential in managing the childhood associated bone mineral density loss that is seen in cystic fibrosis patients. The GP minimises this barrier by having a system that ensures Ruth attends her check-ups and appointments. Although cystic fibrosis cannot be cured there are several treatment options. This can cause damages to various parts of the body such as the skin, kidneys, joints, blood, and brain. Other pulmonary physical signs are dry or productive cough, increased anterioposterior chest diameter, clubbing, cyanosis, and percussion. The CFTR genes are inherited from the parents. Therefore, people with other types of mutations are not eligible to participate in that trial.
From this analysis, it is clear that the research article has provided evidence of a possibility of finding drugs that will target certain aspects of molecular biology of the disease. The discoveries made from researching this disease may very well help the treatment or cure of other, unrelated diseases. This helps these sets of patients to improve their lung functions and also the associated increased exacerbations. Although it is mostly mild in adults, the disease can be fatal in children. Paints often develop difficulty breathing, cough, and wheezing.
It is most common among nations in the Western world minus the exception of Finland but it is equally diagnosed between male and female. Learn More Experimental design It is worth noting that this study was done on laboratory animals as opposed to humans, given that the study on the specific drugs was still underway. High dosages or extended usage of antibiotics can also increase the chances of developing C. With improved ways and early detection, there can be effective ways for managing the condition. The secretions plug up tubes, ducts and airways in the lungs and pancreas. The variation in the clinical manifestation is usually by the age of the patient, especially the age at presentation.
Strengths And Weaknesses Of Family Theory 1359 Words 6 Pages This model is interesting because it is one of the most commonly used models and was created within the clinical setting. I chose recent journal publications and systematic reviews. Cystic fibrosis is the classic example" p. Cystic fibrosis changes the cells that make mucus, sweat and digestive juices. Cystic Fibrosis Could you Imagine what it would be like if you had a disorder that clogged and blocked the passageways in your body? The reproduction of CFTR hinders the chloride channel from its production of chloride ions in cell membranes. In this essay the three main causes of oedema will be explained, the pathophysiology, the intensity factors and the management in a pre-hospital setting. Summary: San Joaquin Valley Fever 660 Words 3 Pages It can develop many years after the fungal infection occurred.
The diet and exercise is also essential for the management of the condition. Gene Therapy for Cystic Fibrosis Cystic fibrosis is one of the most common lethal mutations in humans. They need to know these things because COPD is chronic and the person under our care may die from the disease. The researchers developed and carried out this research study at the research centre growth and signalling, faculty of medicine of the University of Paris Descartes, Paris. Lupus can affect different parts of the body including the skin, blood, kidneys, and joints.
Compared to many of my peers I find myself to be more ambitious and dedicated to my goals. In patients with the condition, the findings observed is that that CFTR gene produces some proteins that are not effective in their function. Among those factors are provider reimbursement and the different types of financial methods used by the patients to acquire healthcare services. The strategy is somewhat different from the older method or style of management simply because the older methods depend on focusing on the symptoms of the lesion as it appears. This results into loss of elasticity, muscle integrity, and cartilage. Using gravity, the thick mucus forces itself down thereby reducing the quantity in the chest. I did use some academic databases like NCBI.
Cystic Fibrosis Essay Chronic illness can be very difficult to manage. Over time, this mucus clogs your passageways which eventually leads to infections. Here are the conditional means: Therapy: People with cystic fibrosis need a way to physically remove thick mucus from their lungs. The CFTR gene deficiency also affects some other parts of the body in various ways. Statistics show that 30,000 people in the US have been named with this disease.