Cystic Fibrosis Essay

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    Cystic Fibrosis

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    Can viruses used as vectors in the process of gene therapy 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, 2017). Since it is recessive, you need two copies of the gene to manifest the disease, but 1/30 Americans have at least one copy

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    Cystic fibrosis is an existence restricting autosomal recessive disorder that influences 70,000 people around the world. The condition is known to affect principally those of European descent, though cystic fibrosis has been accounted for in all races and ethnicities. [12] Unusually viscous emissions in the airway of the lungs and in ducts of the pancreas in people with cystic fibrosis cause hindrances that prompt aggravation, tissue harm and destruction of both organ systems. Studies show that Cystic

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    Introduction Cystic fibrosis Cystic fibrosis (CF) is a lethal autosomal recessive disorder with a clinical incidence of 1 in every 3500 newborns1. Currently, over 4000 Canadians have CF, with 60% being adults2. In the past, CF was considered a fatal disease with a life expectancy of less than two years, however, advances in enzymatic and antibiotic therapy have greatly improved the life expectancy of patients afflicted with CF3. Currently, the median age of Canadian CF patients is 50 years2. CF

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    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

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    Cystic fibrosis is a autosomal recessive inherited disease that affects many organ systems. Over time the outcome for patients with the disease has improved drastically. The life expectancy for patients has increased to 37 years old, compared to 31 years old (O’ Sullivan, 2009). 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

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    reasons. An example of one of these disease is Cystic Fibrosis(CF). There is not much popularity associated with Cystic Fibrosis because there’s limited research on the topic. However, according to the Cystic Fibrosis Foundation, C.F. is a genetic disease that is essentially a severe cold that never goes away. Mucus builds up in the lungs as well as the pancreas and can impair a persons breathing capabilities (About Cystic Fibrosis 1). Cystic fibrosis is a

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    Cystic Fibrosis : A Defect

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    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 RAD212: Image Evaluation and Pathology Abstract What is Cystic Fibrosis? How does it affect people living with it? Cystic Fibrosis, also known as CF, is a life-threatening hereditary disease. It is inherited by a faulty cystic fibrosis transmembrane conductor (CFTR) gene

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    Essay on Cystic Fibrosis

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    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

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    Essay on Cystic Fibrosis

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    Cystic Fibrosis Cystic fibrosis is the most common lethal inherited disease, affecting about 30,000 patients worldwide. In the past decade, strides in patient management and the development of new pharmacological agents, coupled with scientific and technological advances, have increased the mean life expectancy of CF patients to approximately 30 years of age (approximately 50% of CF patients live to the age of 30). As early as 30 years ago, the median survival age was 8 years. Chronic

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    Cystic Fibrosis Cystic fibrosis is described as a “congenital disorder affecting exocrine gland function, with respiratory effects, including excessive secretions, obstruction of the bronchial system, infection, and tissue damage” (Kowalczyk, 2014). Cystic fibrosis is also known as CF, and is the most common lethal disease in white children (Kowalczyk, 2014). People whom have CF have “histologically” normal lungs at birth. Lung damage occurs when secretions from the enlarged bronchial glands gradually

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