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Cystic Fibrosis is usually present the worst in the respiratory system, and the digestive tract. CF can only be obtained by this single defective gene on the number 7 chromosome. Symptoms of this disease are able to be caught pretty early, starting with frequent airway infections, constant coughing, wheezing, abnormal metabolism(excessive amounts of food, with no weight gain), smelly and large feces, and pneumonia. A high level of salt in perspiration is an easy way to tell if a person has this disease. Every new born child now has a 1 in 3,300 chance of getting this disease, with 1 out of every 29 people are carriers...
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Common topics in this essay:
- Autonomy of the patient
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