Cystic Fibrosis Essay Words | 5 Pages Cystic Fibrosis is a severe hereditary disease that infects the lungs, digestive system, sweat glands and male fertility. The name Cystic Fibrosis derives from the Fibrous scar tissue that develops in the pancreas 26/2/ · Cystic Fibrosis (CF) is genetically inherited through a defective gene, which results in the body producing "abnormally thick and sticky fluid, called mucus. This mucus builds up in the breathing passages of the lungs and in the pancreas, the organ that helps to break down and absorb food." (PubMed Health, ) 4/8/ · Aug 4, in Medicine Essay. Cystic fibrosis is a recessive, genetic illness, which affects the work of lungs, liver, intestine, and pancreas. This disease causes malfunctioning of the chloride and sodium transportation across the body and results in the thick and viscous secretions. Nowadays, cystic fibrosis affects thousands of people, Estimated Reading Time: 7 mins
Cystic Fibrosis Essays: Examples, Topics, Titles, & Outlines
Can viruses used as vectors in the process of gene cystic fibrosis essay be an effective treatment for Cystic Fibrosis? Firstly, Cystic Fibrosis is a genetic and recessive disease that mostly affects the lungs and pancreas. This leads to phlegm accumulation, salty sweat, male infertility, shortness of breath and increased risk of infection, which all contribute to premature death CFF, person with Cystic Fibrosis.
Cystic Fibrosis is a disease that forces a person to drown in mucus that fills their lungs while it wreaks havoc on the body. This chronic disease causes devastating health problems, has no cure, and forces patients to endure painful temporary treatments. Taking daily medications, maintaining a social life, and staying moderately healthy are a constant struggle for people with Cystic Fibrosis.
Unlike many of the diseases that plague people today Cystic Fibrosis. Cystic fibrosis is also known as CF, and is the most common lethal disease in white cystic fibrosis essay Kowalczyk, Lung damage occurs when secretions from the enlarged bronchial glands gradually. Cystic Fibrosis is a severe hereditary disease that infects the lungs, digestive system, sweat glands and male fertility.
The name Cystic Fibrosis derives from the Fibrous scar tissue that develops in the pancreas. First recognized incystic fibrosis is generalized as an autosomal recessive disorder of the exocrine glands, cystic fibrosis essay.
About one in every Caucasians is affected, and one in 25 is a carrier of the cystic fibrosis gene. Cystic fibrosis is the most common fatal hereditary. Running head: Cystic Fibrosis: A Defect in the CFTR Gene Cystic Fibrosis: A Defect in the CFTR Gene Alexandra L Allen Southern Union State Community College RAD Image Evaluation and Pathology Abstract What is Cystic Fibrosis?
How does it affect people living with it? Cystic Fibrosis, also known as CF, cystic fibrosis essay, is a life-threatening hereditary disease. It is inherited by a faulty cystic fibrosis transmembrane conductor CFTR gene. Cystic Fibrosis Cystic fibrosis is the most common lethal inherited disease, affecting about 30, patients worldwide. As early as 30 years ago, the median survival age was 8 years.
The following are a few common myths and truths about Cystic fibrosis essay Fibrosis: Cystic Fibrosis is contagious. False, CF is not contagious. It is a disease that is genetically inherited by the child from his or her parents who either have the gene or are carriers of the gene, cystic fibrosis essay. The gene that codes for Cystic Fibrosis has been found, cystic fibrosis essay.
True, the gene that produces the cystic fibrosis transmembrane conductance regulator protein, CFTR, is known. A defect in this protein. Cystic fibrosis is an autosomal recessive genetic disorder characterised by a mutation in the cystic fibrosis transmembrane conductance regulator CFTR protein which acts as a chlorine channel that regulates water and ion levels across the epithelia.
Cystic fibrosis can affect sweat glands, the respiratory system, digestive system and the reproductive system. In the lungs defects in the CFTR protein results in airway surface liquid depletion, triggering a cascade of events resulting in infection, cystic fibrosis essay. Cystic fibrosis is due to a mutation in the gene that encodes cystic fibrosis transmembrane conductance regulator CFTR protein. It effects the exocrine glands which are responsible for making mucus and sweat.
It causes a thickening of the mucus in your body and increases the salt content of your sweat. These can lead to problems including problems absorbing oxygen, lung infections, inhibit digestive enzymes from reaching your small intestine, dehydration, increased heart rate, lower blood pressure. Cystic fibrosis is a autosomal recessive inherited disease that affects many organ systems, cystic fibrosis essay.
Over time the outcome for patients with the disease has improved drastically. Researchers have reviewed the etiology, pathogenesis and clinical manifestations for cystic fibrosis. The cause of Cystic Fibrosis is mutations in a single gene on chromosome 7 that encodes for the cystic fibrosis transmembrane. Home Page Research Cystic Fibrosis Essay.
Cystic Fibrosis Essay Words 4 Pages. The contaminated lungs will produce mucus that is thick cystic fibrosis essay adhesive which clogs the lungs and leads to an unpleasant and abhorrent lung infection. CF also interferes with the pancreas, disallowing the digestive enzymes from breaking down and absorbing food in the intestine. This can result in low nutrition, feeble growth, excessive sweat production, cystic fibrosis essay, difficulties in breathing, and sometimes lung disease.
When producing extra sweat and mucus, the body loses salt. If too much salt is lost, it can cause abnormal heart rhythms, disturbance of minerals in the blood, and perhaps, shock, cystic fibrosis essay. But more than eighty percent of the patients are diagnosed by age three. Today, nearly forty percent of the diagnosed inhabitants are at the age of eight-teen or older. Today, there is no cure for Cystic Fibrosis, but if the cystic fibrosis essay is found in an individual early enough, the patient can be recovered.
And because enzymes are lost when diagnosed, enzyme supplements are required to prevent bad nutrition and malnutrition. There are two cystic fibrosis essay body parts that can be cared for the treatment of Cystic Fibrosis: The lungs and the chest. Lung problems can also be treated, but not cured. Antibiotics and other drugs may loosen the thick mucus in the lungs, cystic fibrosis essay, but if it fails, a transplant lung may help to extend life.
But about four hundred people die each year while waiting for a lung transplant. Also Chest physical therapy is a technique done by vigorous claps on the back and chest to loosen the thick mucus from the lungs. The average lifespan of an individual with CF is about thirty years, cystic fibrosis essay.
In the U. S alone there are about thirty cystic fibrosis essay, who are carriers of the disease, and about 2, babies are born with it each year. About cystic fibrosis essay percent of the Americans are unaffected carriers who may discover symptoms later in their lifetime. CF occurs mainly in. Get Access. Cystic Fibrosis Words 4 Pages Can viruses used as vectors in the process of gene therapy be an effective treatment for Cystic Fibrosis?
Read More. Essay on Cystic Fibrosis Words 8 Pages person with Cystic Fibrosis. Cystic Fibrosis Essay Words 5 Pages Cystic Fibrosis is a severe hereditary disease that infects the lungs, digestive system, sweat glands and male fertility. Cystic Fibrosis : A Defect Words 14 Pages Running head: Cystic Fibrosis: A Defect in the CFTR Gene Cystic Fibrosis: A Defect in the CFTR Gene Alexandra L Allen Southern Union State Community College RAD Image Evaluation and Pathology Abstract What is Cystic Fibrosis?
Essay on Cystic Fibrosis Words 5 Pages Cystic Fibrosis Cystic fibrosis is the most common lethal inherited disease, affecting about 30, cystic fibrosis essay, patients worldwide. Cystic Fibrosis Essay Words 16 Pages The following are a few common myths and truths about Cystic Fibrosis: Cystic Fibrosis is contagious.
What is Cystic Fibrosis? A Study On Cystic Fibrosis Words 5 Pages Cystic fibrosis is due to a mutation in the gene that encodes cystic fibrosis transmembrane conductance regulator CFTR protein. The Cause Of Cystic Fibrosis Words 4 Pages Cystic fibrosis is a autosomal recessive inherited disease that affects many organ systems.
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Cystic Fibrosis and the Mucociliary System
, time: 6:10Cystic Fibrosis Essay | Rebecca Grainger - blogger.com
12/4/ · Cystic Fibrosis Essay Introduction: Cystic fibrosis (CF) also known as mucoviscidosis is an inherited disease that causes the body to produce mucus that's extremely thick and sticky. The mucus in people with CF is thicker than normal because CF affects cells in the epithelium, the layer of cells that lines the passages in the body's organs 26/2/ · Cystic Fibrosis (CF) is genetically inherited through a defective gene, which results in the body producing "abnormally thick and sticky fluid, called mucus. This mucus builds up in the breathing passages of the lungs and in the pancreas, the organ that helps to break down and absorb food." (PubMed Health, ) 4/8/ · Aug 4, in Medicine Essay. Cystic fibrosis is a recessive, genetic illness, which affects the work of lungs, liver, intestine, and pancreas. This disease causes malfunctioning of the chloride and sodium transportation across the body and results in the thick and viscous secretions. Nowadays, cystic fibrosis affects thousands of people, Estimated Reading Time: 7 mins
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