CHECK THESE SAMPLES OF Aminoglycoside and Hearing Loss in Children with Cystic Fibrosis
Medical archives indicate that, among the litany of genetic diseases known to affect man, cystic fibrosis constitutes one of the thoroughly researched and understood diseases.... cystic fibrosis has been identified as a progressive disorder that affects thousands of people and often results to fatalities.... To better provide insight of cystic fibrosis, an intricate understanding is essential on its historical evolution, causes, signs and symptoms, prevalence rates, treatment and management....
10 Pages
(2500 words)
Research Paper
Existence of cystic fibrosis has been known for a very long time from stories of old cleaning ceremonies where foreheads of children were licked to see if they were salty and if they were those children were feared to die soon due to the disease which we today call cystic.... Other significant report of pancreatic changes with features compatible to that of cystic fibrosis came from Margaret Harper of Sydney who reported congenital steatorrhea due to pancreatic defect (Harper, 45-56)....
4 Pages
(1000 words)
Research Paper
In people with cystic fibrosis the defective gene inhibits the reabsorbing of chloride and sodium ions resulting in an excess of sodium chloride or very salty sweat.... In the respiratory tract of persons with cystic fibrosis there is a reduction of the secretion of sodium ions and water caused from the inability of epithelial cell membranes to influence the hydration of mucus.... While in some people the It is possible that several hundred different mutations of the gene exist than can cause cystic fibrosis....
11 Pages
(2750 words)
Essay
The gene in question is called cystic fibrosis transmembrane conductance regulator (CFTR) which normally expresses a protein that helps chloride ions move in and out of epithelial cells lining.... Furthermore, cystic fibrosis also causes too much salt to be excreted in the sweat glands, resulting in electrolyte imbalance.... he pattern of inheritance for cystic fibrosis is homozygous recessive.... he standard approach to the diagnosis of cystic fibrosis is made by measuring the chloride content of an individual's sweat....
2 Pages
(500 words)
Essay
he following paper will examine cystic fibrosis through looking at what is known about the disease in relationship to its pathology, through the developing knowledge that has increased life expectancy, and through the treatments and care that has extended the lives of those who suffer from the illness.... cystic fibrosis is a devastating disease that has taken the lives of many children, but with the advances that have been made in understanding the disease, people are now living much longer and more meaningful lives as they live with the condition....
14 Pages
(3500 words)
Research Paper
The CFTR protein in people without cystic fibrosis controls the flow of salt and water through the epithelial walls.... A cystic fibrosis patient who has a mutated CFTR gene, the passage of sodium chloride through the epithelial cells does not occur normally.... In addition, thick and sticky mucus, which is the main symptom in cystic fibrosis patients, clogs the bronchioles and as a result, parts of the lungs become blocked off.... ystic fibrosis causes acute respiratory problems; this is due to acute haemoptysis and pneumonia....
5 Pages
(1250 words)
Essay
Parents who give rise to offsprings with cystic fibrosis might not have the disease themselves.... Parents who give rise to offsprings with cystic fibrosis might not have the disease themselves because each parent gives two genes that are faulty to their children.... atients with cystic fibrosis, mutation of cystic fibrosis transmembrane conductance regulator is unable to control the epithelial sodium channel (ENaC).... ucus provides a lining cavity to the organs, and individual suffering from the disease has mucus that is sticky number cystic fibrosis What is cystic fibrosis?...
2 Pages
(500 words)
Essay
In the United States, there are an estimated 30,000 individuals diagnosed with cystic fibrosis ('About cf,' 2014).... The paper "cystic fibrosis Lung Transplantation" utilizes evidence and factual data that many lives have been saved from the transplantation and the earlier prevention or earlier diagnosis of the disease as this will help the patient keen on drugs and body maintenance.... cystic fibrosis is a genetic disease with no cure at this time....
15 Pages
(3750 words)
Research Paper