A comprehensive overview of the hereditary lung disease, cystic fibrosis.
Written in 2004; 2,625 words; 9 sources; MLA; $ 79.95
Paper Summary:
This paper discusses the hereditary lung disease, cystic fibrosis (CF). The paper presents statistics of those suffering from CF in the United States. The cause, symptoms and diagnosis of the disease are examined. The paper explores the prognosis for CF patients and analyzes the available treatments. The paper contends that although much progress has been made in recent years in terms of diagnosis, treatment, quality of life, as well as average life spans, there is clearly much more to be done.
Outline
Introduction: What is Cystic Fibrosis?
Incidence and Etiology
Pathology and Pathophysiology
Signs, Symptoms and Complications
Diagnosis
Prognosis
Treatment
Clinical Trials and Studies
Hidden Benefits
Conclusion
From the Paper:
"Cystic fibrosis is a serious genetically inherited disease that is estimated to affect around 30,000 children and adults in the United States alone (CFF, 2005). In this disease, a defective gene causes parts of the body to produce abnormal sticky, thick mucus. This abnormal mucus causes the lungs to become clogged, and can also lead to serious lung infections that can be fatal (2005). In addition to the negative effect on lung function, the thick mucus also causes an obstructive barrier to the pancreas which results in the patient having difficulty with food digestion as well as nutrient absorption. Cystic Fibrosis can cause complications leading to early mortality (the average age of the Cystic Fibrosis patient today is 30). Yet advances in treatment have steadily increased life the life expectancy of people suffering from this disease."
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