March 4‚ 2013 Cystic Fibrosis Hey‚ My name is Ivy Clements and today I will be informing you all about Cystic Fibrosis. How many of you know what Cystic Fibrosis is? Well today I am going to inform you on what Cystic Fibrosis actually is. I am going to start off this speech by telling you about Cystic Fibrosis‚ then I am going to tell you some of the signs and symptoms‚ and I am going to end with telling you a few facts and figures about this disease. Cystic Fibrosis is one of the most
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for Cystic Fibrosis Cystic Fibrosis‚ also called CF‚ is the most common life threatening disorder in the US. It is an inherited disease of the secretory glands (National Blood‚ Heart and Lung Institute‚ 2013). Affecting about 30‚000 people‚ it is an autosomal recessive disorder due to mutations in the CF transmembrane conductance regulator (CFTR) gene (National Blood‚ Heart and Lung Institute‚ 2013). Usually diagnosed at a young age‚ CF causes the mucus‚ sweat and digestive fluids to become thick
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Case Study On Cystic Fibrosis. Biology Research 265 Jerry Harris Dr. Kathy Durham Question One: The physician asked the mother of the infant if the infant’s skin was salty because one of the symptoms of cystic fibrosis is having thick and heavy mucous ... and salty sweat. When the CFTR (Cystic Fibrosis Trans membrane Conductance Regulator) protein is defective‚ epithelial cells can’t regulate the way chloride (part of the salt called sodium chloride) passes across cell membranes. This
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inherently‚ has developed quite the propensity for taking things for granted. Whether it be indoor plumbing‚ air conditioning‚ eating on a daily basis‚ or having clean socks to wear‚ you can bet we don’t appreciate it like we should. The majority of the population carries on their whole life like this; totally ignorant of how truly lucky they are. Then‚ there’s a small piece of the pie that is born‚ for lack of a better word‚ unlucky. Very‚ VERY unlucky. I just so happen to be closely related to one of
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Introduction: Cystic fibrosis (CF) is the most common inherited disorder which results from mutation of cystic fibrosis transmembrane regulator (CFTR) gene. It occurs approximately in one of every 2500 live births in the white population(1) ; and characterized by abnormal thick viscous secretions in the respiratory‚ gastrointestinal and genitourinary tracts together with chronic suppurative endobronchial infection(2)‚ resulting in death or lung transplantation in more than 500 patients every year
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A Nursing Diagnosis for Cystic Fibrosis Nursing diagnoses describe problems that can be addressed by nursing measures. Because nurses can ’t diagnose a disease or prescribe medication‚ a nursing diagnosis doesn ’t describe a disease or prescribe medications or treatments beyond a nurse ’s scope of practice. In the case of a disease like cystic fibrosis‚ nursing diagnoses center on treating problems caused by the disease. Description According to the North American Nursing Diagnosis Association
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abies born with CF don’t gain weight as expected. They fail to thrive in spite of a normal diet and a good appetite. Mucus blocks the passageways of the pancreas and prevents pancreatic digestive juices from entering the intestines. Without these digestive juices‚ the intestines can’t absorb fats and proteins completely‚ so nutrients pass out of the body unused rather than helping the body grow. Poor fat absorption makes the stools appear oily and bulky and increases the child’s risk for deficiencies
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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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Cystic fibrosis is a crippling disease that affects thousands of people worldwide. Cystic fibrosis is an inherited disease of the secretory glands that causes persistent lung infections and limits the ability to breathe over time. It causes cells to produce thick and sticky mucus‚ sweat‚ and digestive juices that block airways‚ ducts‚ and passageways. There is no cure‚ but there are ways to manage symptoms. According to the World Health Organization‚ the occurrence of cystic fibrosis varies across
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------------------------------------------------- Introduction Cystic fibrosis (also called CF or mucoviscidosis) is an autosomal recessive genetic disorder that affects most critically the lungs‚ and also the pancreas‚ liver‚ and intestine. It is characterized by abnormal transport of chloride and sodium across an epithelium‚ leading to thick‚ viscous secretions. The name refers to the characteristic scarring (fibrosis) and cyst formation within the pancreas that was first recognized in the
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