Cystic Fibrosis What is Cystic Fibrosis? Cystic fibrosis is a disease passed down through families that causes thick‚ sticky mucus to build up in the lungs‚ digestive tract‚ and other areas of the body. It is one of the most common chronic lung diseases in children and young adults. It is a life-threatening disorder. Causes It is a disorder that occurs due to mutation in the Cystic Fibrosis Transmembrane Conductance Regulator {CFTCR} gene. This gene codes for a product that influences the production
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Eventually if the cystic fibrosis gets worse‚ a lung transplant will be a necessity. This disease is not deadly unless not treated in time. In this report‚ there will be a discussion of several topics described throughout the paper to name a few topics: Background on Cystic Fibrosis‚ causes‚ symptoms‚ treatments and prevention. Background Dr. Dorothy Anderson was born in Asheville‚ North Carolina on May 15‚ 1901. She was the only child to both of her parents Mr. and Mrs. Anderson. At a young
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Cystic Fibrosis is a severe inherited disease that affects 30‚000 children each year in the United States. As the disease is inherited‚ it is created by a mutated protein that regulates the equilibrium of salt in each cell. This mutated protein affects the normal function of Epithelial Cells or sweat cells and cells that line the lungs. This defected epithelial cell creates a thick and sticky mucus that can impair the flow of oxygen to the lungs. CF is a chronic disease that can affect every aspect
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There is an estimated 30‚000 people in the United States that have Cystic Fibrosis (CF) and about 25 million who have asthma. CF is often confused with asthma because of their symptom similarities. CF‚ despite what people may think is far more severe than asthma. Most people think that CF would be easier to treat and cure because there are fewer people with it. Unfortunately‚ at this point there is no cure for CF. Cystic Fibrosis is far more severe than asthma because it is terminal‚ the treatment
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called cystic fibrosis. Cystic fibrosis is a life threatening disease that can cause mucus in the lungs and intestines. Cystic fibrosis is a genetic disease that causes mucus to block the intestines and lungs.When you have Cystic fibrosis the normally thin liquid mucus in your lungs and intestines turns into a thick and sticky substance trapping bacteria causing infections and blocking passageways. The usually thin mucus is supposed to act as a lubricant. When the thick mucus is in your body it
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Krickett Davis Zachary Mock Cystic Fibrosis Case Study: Part I Questions: The Meeting Consult your textbook and trustworthy Internet sites to answer the following questions: 1. Which organs are affected by cystic fibrosis? What are the disease symptoms? Organs that are affected by cystic fibrosis include the lungs‚ pancreas‚ liver‚ sweat glands‚ reproductive organs‚ nose and sinuses. The symptoms of cystic fibrosis include coughing with mucus coming up‚ wheezing‚ breathlessness‚ decrease in ability
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Cystic Fibrosis is caused by a fault in the cystic fibrosis transmembrane conductance regulator (CFTR) gene on chromosome 7 at q31.2. For CF to be expressed‚ a faulty copy of the gene must be present at both alleles; autosomal recessive. Therefore both parents must be carriers of‚ or affected by the cystic fibrosis gene (fig. 1) for the gene to be passed on. If a person has one copy of the faulty allele (are heterozygous) they are carriers of the gene and can pass this allele on; if they possess
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Physiology of Cystic Fibrosis Samantha J. Cordova Pueblo Community College Abstract The main topic researched in this paper is cystic fibrosis. The research in detail is that cystic fibrosis is classified as a genetic disorder and in what ways this disorder affects the gene expressions. More facts found in this paper will be who can get cystic fibrosis‚ which organs are mostly affected‚ and what specifically causes the problems found from cystic fibrosis. Common symptoms from this disorder can
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Cystic Fibrosis Julie LeBeau Mildred-Elley BIO 210 February 20‚ 2014 Cystic Fibrosis Cystic Fibrosis is a fatal genetic disorder that effect’s many organ systems in the body. It is estimated that CF effects 30‚000 adults and children in the United States‚ with approximately 1‚000 new cases diagnosed each year. Cystic Fibrosis is most prevalent among white but affects all ethnic groups. Cystic Fibrosis results from an autosomal recessive gene mutation of the Cystic Fibrosis transmembrane
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Cystic fibrosis is a chronic lung disorder caused by an autosomal recessive multiorgan disorder. The disorder is due to an exocrine gland dysfunction. The deficiency in chloride flow and increase sodium absorption results in thick sticky mucous that clogs the lungs and obstruct glands The pancreas obstruction leads to the failure of secretion of enzymes. The chronic lung disorder is prevalent amongst Caucasians. “Cystic fibrosis occurs in one of 2‚5000Caucasians‚approximately 30‚000 individuals
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