Cystic fibrosis research paper

In fact, this symptom of not being able to absorb nutrients or digest foods causes many other symptoms. These function to measure the size of the lungs, the speed and capacity of air they can breathe in and out, and how well the lungs are delivering oxygen to the blood.

One in every seventeen-thousand African Americans is a carrier of the mutated gene, and one in thirty-thousand Asian-Americans is a carrier. With the knowledge of this gene, scientists could also, for the first time, synthesize a healthy version of the gene for research.

A bronchodilator helps to relax the muscles and keep airways open. However, many different medications and activities help to lower chances of harmful symptoms of cystic fibrosis and help to prevent certain fatal events from occurring.

About one in every twenty-five Americans of European descent is a carrier of the gene, though possibly not infected fully with cystic fibrosis. Without the movement of the chloride ions, the mater and mucus cannot move out, causing a buildup of mucus.

Women with CF may also be less fertile than women without CF. One of the most common of these mutations is a deletion of a single amino acid from the long chain of in the CFTR protein.

Most Downloaded Journal of Cystic Fibrosis Articles

The hereditary disease eventually leads to disability and multisystem failure due to the effects this mucus. Pathological changes in lungs are characterized the signs of chronic bronchitis with development of bronchiectasis and diffuse pneumosclerosis.

Cystic Fibrosis Research Paper Essay

In order to get CF, both partners must be a carrier because the CF gene is recessive. A genetic test usually begins with a blood sample or a cell sample taken from inside the cheek.

Cystic Fibrosis Research Paper

Mucus thinning drugs help to reduce the stickiness of mucus, improving lung function. Gene Without the cystic fibrosis variation of the CFTR gene, the CFTR proteins created by the gene act as a channel protein which can be found in the membranes of cells which line the passageways of organs such as the pancreas, lungs, and intestines.

There is no known cure for cystic fibrosis. If someone with a family history of Cystic Fibrosis is thinking about having a child, they might want to undergo genetic testing before having children of their own.

In the yearpatients with cystic fibrosis had a median or average life span of about ten years. Thus eventually resulting in the formation of the sweat test which is now the standard test.

Hire Writer They can also have an electrolyte imbalance because they have saltier sweat which upsets the balance of minerals in their blood. A person with CF should exercise regularly, stay away from smoke, and encourage hand washing to the whole family.

Treatment of cystic fibrosis: In the lungs, the airways become clogged, patients experience difficulty breathing and they become susceptible to bacterial infections.

Several tests are also used to monitor disease progression and identify any complications that may occur. Furthermore CF causes the sweat glands to release about 5 times6 as much salt as a normal person would. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.

Cystic Fibrosis tends to run in families, since it is an inherited disease. InDorothy Andersen M. If someone is a carrier, they could pass it on to their own child. D kalo ada essay gmna coba?? College and university writers looking for preparing interesting and argumentative research proposal on cystic fibrosis have to do their best to take into account all the various aspects of the given topic and make all their efforts to bring some new ideas on the subject.

Because cystic fibrosis is a hereditary disease, different populations are more or less likely to have this mutation in the CFTR gene.Cystic fibrosis or mucoviscidosis is a systemic inherited disease, caused by the mutation of cystic fibrosis transmembrane conductance regulator (CFTR) and characterized by exocrine gland involvement, and heavy disorders in the functions of breathing organs.

The Cystic Fibrosis Foundation (CFF) is currently the worldwide leader in the search for a cure for CF patients by funding promising research and working to provide access to quality, specialized care and treatments. CFF works under a venture philanthropy model that provides early stage funding to biotechnology and pharmaceutical companies for the development of breakthrough drugs for adults.

Cystic Fibrosis can cause problems in the reproductive system. Cystic Fibrosis patients have many more sexual reproduction problems than a healthy human.

Cystic Fibrosis Research Paper

In males with CF, they are likely to be infertile because of the tube connecting the testes and the vas deferens is missing or blocked with mucus. Understanding Cystic Fibrosis: The Basics - WebMD.

Cystic Fibrosis Research

The Effects of Cystic Fibrosis on the Patient - Congenital Disability Paper: Cystic Fibrosis Ashley Cooper University of Northern Colorado Congenital Disability Paper: Cystic Fibrosis Cystic Fibrosis is a somewhat rare and unfortunate illness that few people will battle.

In a group of parents founded the Cystic Fibrosis Foundation, which later became the National CF research Foundation in as well. In ,b The foundation created the Research Development Program, which is a network of research centers at top universities.

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Cystic fibrosis research paper
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