Urea cycle disorder Report
Urea cycle disorder
Urea cycle disorder is a group of rare genetic disorders that affect the body's ability to remove ammonia from the blood. Urea cycle disorders are caused by mutations in genes involved in the urea cycle, and this report tests for genetic variants that are known to affect these processes.
More than 10 genes analyzed
It is recommended if:
This report is designed for individuals with a family history of urea cycle disorders or individuals with symptoms of the condition, such as lethargy, vomiting, and seizures. 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:
- Argininemia
- Argininosuccinic Aciduria
- Citrullinemia
- N-acetylglutamate synthase deficiency
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!
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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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