Cystic fibrosis research paper essay

Also medicated vapors are inhaled and open clogged airways. Chloride levels that are above a certain threshold indicate that the person has CF. In some cases this malnutrition causes people to die when they are only children.

This is one issue that has been heavily debated in the past.

Cystic Fibrosis

Currently, even through years of research and progress, there is no true cure for cystic fibrosis. Then the pad is wrapped in plastic and is sent to a lab to get analyzed.

Patients with CF will also take pills called pancreatic enzyme supplements before meals and snacks since the disease blocks pancreatic enzymes from getting into the intestines.

There are now many drugs that are in the market and many more that are in development. Often, the techniques use vibrations to help loosen the mucus in the lungs so it can be coughed out.

When folded improperly, the substances for which the protein was made cannot fit through the protein channel, and so cannot pass through it. The fact that the disease presents in epithelial cells of patient's airways should be a worry to the healthcare practitioners.

Cystic fibrosis is caused by a mutation in a gene called the cystic fibrosis transmembrane conductance regulator CFTRwhich serves an important function in creating sweat, mucus, and digestive juices.

Now there are many tests that can be done to find put if a person has CF. Try adding some vegetables, such as onions or spinach.

Adults with cystic fibrosis tend to live longer and therefore develop non-respiratory symptoms. In a CF patients the lungs become covered with a sticky mucus that is hard to remove and promotes infection from bacteria.

There are other mutations that mainly occur in non-white populations Scott, Also it is more common for people with cystic fibrosis to develop digestive tract cancer7. There are now many studies that the medicine ibuprofen Advil, Motrin IB, Nuprin prevents serious damage to lungs in children who have CF.

Such tests include prenatal genetic testing, ultrasonography, and amniocentesis. How does a person know if they have CF? Cystic fibrosis is a hereditary disease in that one can only get it if his or her parents both are carriers.

Essay/Term paper: Cystic fibrosis

Many years ago, New York4 had a heat wave, and the hospitals became overwhelmed with dehydrated CF children. Patients with cystic fibrosis are subjected to medical imaging examination as it helps in monitoring the disease pathologic changes.

High dose ibuprofen can be used to inhibit lung deterioration.

Cystic Fibrosis - Research Paper Example

This is caused by the other symptom of not being able to digest foods and retain nutrients. The phenotype or physical appearance of anyone with the autoimmune disease cystic fibrosis varies, as there are multiple possibilities and combinations, but have many recurring traits.

This is why the skin of a CF patients may taste salty. The overproduction of mucus causes the pancreatic ducts to be clogged.

It disrupts the body's salt balance, leaving too little salt and water on the outside of cells and causing the thin layer of mucus that usually keeps the lungs free of germs to become thick and sticky.

The options are to: Early detection of cystic fibrosis in children has massive health benefit to these children especially under circumstances when neonatal screening is used to diagnose the disease. Collins from University of Michigan. Other method used is sinus imaging that is used to ascertain degree of sinus impairment.

Most Downloaded Journal of Cystic Fibrosis Articles

Due to the high concentration of the enzymes the end result is deterioration of the pancreas leading to diabetes. PubMed Health, Reported as lung-related symptoms are those stated as follows: Cystic Fibroids Cystic fibrosis Cystic fibrosis is a disease that can be passed down from one generation to the other.

Symptoms of cystic fibrosis: This treatment is when the patient is hit on the back and chest with cupped hands to loosen the mucus so it can be coughed up easier. Cystic fibrosis was discovered in the s by the Bohemian pathologist Carl von Rokitansky, who made the first description of the disease as part of a report about a death of a fetus.Excerpt from Research Paper: Cystic Fibrosis (CF) is genetically inherited through a defective gene, which results in the body producing "abnormally thick and sticky fluid, called mucus.

The disease can be fatal without proper treatment, because unfortunately there is no cure. Every day three people die from cystic fibrosis. This makes cystic fibrosis the most deadly out of 4, different inherited diseases.

Cystic Fibrosis

Over 30, children and adults in the United States have cystic fibrosis. Read this Science Essay and over 88, other research documents. Cystic Fibrosis.

Cystic Fibrosis Cystic Fibrosis is the largest fatal genetic disease in the country, and North America today. Its victims only /5(1). Cystic Fibrosis This Research Paper Cystic Fibrosis and other 64,+ term papers, college essay examples and free essays are available now on Autor: review • February 14, • Research Paper • 2, Words (9 Pages) • 1, Views4/4(1).

Cystic Fibrosis, a very serious inherited genetic disease, is also known as CF and sixty-five roses. This disease affects one in every 3, live births. Cystic Fibrosis This Research Paper Cystic Fibrosis and other 64,+ term papers, college essay examples and free essays are available now on Autor: review • February 14, • Research Paper • 2, Words (9 Pages) • 1, Views.

Cystic Fibrosis Research Paper

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Cystic fibrosis research paper essay
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