Wilson Disease Report
Wilson Disease
Wilson disease is a rare inherited disorder that causes copper to accumulate in the body, leading to liver damage and neurological symptoms. Wilson disease is caused by mutations in a gene involved in copper transport and metabolism.
1 or more genes analyzed
It is recommended if:
This report is designed for individuals with a family history of Wilson disease or individuals with symptoms of the condition, such as liver disease or neurological symptoms. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
List of main conditions:
- Wilson disease
Simple workflow
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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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