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Cystic Fibrosis happens as the result of a genetic mutation during conception. It is not something that you can develop later in life or that you can catch from another person. Everyone's lungs has some mucus inside them to keep them moist and from rubbing on each other. In CF, that mucus is really thick, making it harder for the person to breathe, and easier for them to get infections. As they get older, the problem tends to progress as the lungs get weaker due to repeated infections, and it gets hard to expel all of the excess mucus. Most people end dying by their mid-20's. Also, most of them are diagnosed with "failure to thrive" as an infant/child, meaning that they aren't gaining height and/or weight at the normal rate for their age and gender.

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Q: What actually goes wrong with the body and what are the symptoms when you have cystic fibrosis?
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What resaerch is being done on cystic fibrosis?

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What kind of molecules produce the symptoms of cystic fibrosis?

cystic fibrosis is a genetic code, so its not really molecules that cause it, however its more of a DNA mutation that's happened when your born. this means that your mucus cells don't function properly and when they are created, they are made with the wrong gene coding and so will produce more mucus than they're supposed to which is what forms in the lungs. i think that's right and i hope it helps :)


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