Noonan Syndrome Report
Noonan Syndrome
This report tests for mutations in genes associated with Noonan syndrome, a genetic disorder that affects many areas of the body. Noonan syndrome is characterized by characteristic facial features, short stature, heart defects, and developmental delays. Testing can help diagnose the condition, identify the genetic cause, and inform medical management and support for affected individuals and their families.
More than 10 genes analyzed
It is recommended if:
Individuals who have symptoms of Noonan syndrome or a family history of the condition. This may include individuals with characteristic facial features, short stature, heart defects, or developmental delays.
List of main conditions:
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.
How will I receive my reports?
The first thing to do when you receive your kit is to register it on your Genome Manager account. Dante's proprietary platform will keep you up-to-date on all stages of your genetic journey, providing you with the real-time status of your sample and where you can download your free report and raw data* at any time.
*Raw data will be available free of charge for the first 30 days after release.
How can I add other reports to my account?
At any time, you can log into your Genome Manager account and visit the Shop section. Here you will find a catalog with more than 150 additional reports dedicated to all areas of health. In addition, by subscribing to our newsletter you can always see new reports and panel updates.
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