Cystic Fibrosis Report
Cystic Fibrosis
Mutations underlying Cystic Fibrosis destroy the function of chloride channels, compromising the passage of this ion and of water across cell membranes. As a consequence, the secretion of the exocrine glands will be sticky (with risk of obstruction), while the lungs will produce an excessive amount of mucus.
10 genes analyzed
It is recommended if:
Test particularly indicated for newborns with suspected diagnosis, for potentially carrier subjects (for example, couples who are planning a pregnancy) and for those who have affected relatives, in order to verify their genetic risk.
List of main conditions:
- Cystic Fibrosis
Simple workflow
*To generate this report, a sequencing test is mandatory. If you have not yet acquired a sequencing test, kindly make the purchase at this link: Dante Genome Test now!
Purchase your report adding your kit ID in the checkout notes.*
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FAQs
How will my data be used?
Your data is yours. Which is why we have developed proprietary software linked to a dedicated platform, the Genome Manager, to provide you with unique access to your data whenever you want, wherever you are.
How can my doctor use the results?
You will be provided with a digital version of the raw data and reports. Thanks to these in-depth tools, you will be able to share your preferred information with your geneticist and/or doctor to indicate and plan the healthiest course for you.
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*Raw data will be available free of charge for the first 30 days after release.
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