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A disease that is inherited and endangers the lungs and the digestive system.

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It makes the cells mucas sweat and build up and it causes your airways and other passageways to fill up with thick mucas. Includes coughs and lung infections and the inability to gain weight.

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Cystic Fibrosis is caused by mutations on chromosome 7

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Sweat tests are used to test the levels of salt in someones sweat. If a genetic tests detects two defective CFTR genes, then just one sweat  test may be all you need.

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How many and what type of people are likley to have the disorder? 

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How many and what type of people are likley to have the disorder? 

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1. Its only given to you through genetics so you don't have to worry unless you have a carrier in your family.

2. Its not too common among people but keep in mind that it definitely exists and is still a problem with the many people that have it.

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If only one parent passes down the mutation then you're just a Cystic Fibrosis carrier

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Airway Clearance Techniques, Medications, Lung Transplant, And Treatment plants

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https://www.cff.org/Life-With-CF/Treatments-and-Therapies/
https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/
https://www.mayoclinic.org/diseases-conditions/cystic-fibrosis/symptoms-causes/syc-20353700

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Its a gene mutation that makes it so that protein that doesn't work as intended. The effect in this being that this causes mucas to stock up a lot faster and eventually store itself in the lungs.

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Cystic Fibrosis is not sex-linked and is inherited when someone gets a mutated copy of the gene associated with cystic fibrosis.

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https://www.childrenshospitaloakland.org/main/mackenzie-cystic-fibrosis-story.aspx

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Cystic Fibrosis: Mackenzie's Story | UCSF Benioff Children's Hospital Oakland