Waardenburg Syndrome Report
Waardenburg Syndrome
Characterized by differing levels of hearing impairment and minor structural abnormalities originating from the neural crest, Waardenburg Syndrome (WS) results in irregular pigmentation of the eyes, hair, and skin. WS manifests in four distinct clinical and genetic phenotypes. There is currently no known cure for Waardenburg Syndrome, but individuals with this condition typically have a normal life expectancy and can lead fulfilling lives. However, it is essential to address and manage any symptoms as they arise.
8 genes genes analyzed
It is recommended if:
This report is appropriate for individuals who show clinical indications, symptoms, or have familial suspicions of Waardenburg Syndrome.
List of main conditions:
- Waardenburg syndrome, type 4A
- Waardenburg syndrome, type 4B
- Waardenburg syndrome, type 1
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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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