Cystic fibrosis

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  • Cystic Fibrosis

    983 Words  | 4 Pages

    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

  • Essay on Cystic Fibrosis

    1790 Words  | 8 Pages

    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

  • A Report On Cystic Fibrosis

    945 Words  | 4 Pages

    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

  • Cystic Fibrosis Essay

    1129 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. First recognized in 1938, cystic fibrosis is generalized as an autosomal recessive disorder of the exocrine glands. About one in every 2500 Caucasians is affected, and one in 25 is a carrier of the cystic fibrosis gene. Cystic fibrosis is the most common fatal hereditary

  • Cystic Fibrosis : A Defect

    3451 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 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

  • Essay on Cystic Fibrosis

    1134 Words  | 5 Pages

    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

  • Cystic Fibrosis Essay

    3952 Words  | 16 Pages

    The following are a few common myths and truths about Cystic 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. The gene that codes for Cystic Fibrosis has been found. True, the gene that produces the cystic fibrosis transmembrane conductance regulator protein, CFTR, is known. A defect in this protein

  • What is Cystic Fibrosis?

    903 Words  | 4 Pages

    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

  • A Study On Cystic Fibrosis

    1042 Words  | 5 Pages

    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

  • Introduction. Cystic Fibrosis . Cystic Fibrosis (Cf) Is

    1323 Words  | 6 Pages

    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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