Bartter and Gitelman's Syndromes Report
Bartter and Gitelman's Syndromes
Bartter and Gitelman's Syndromes are a spectrum of inherited tubulopathies sometimes difficult to distinguish, given the sharing of some characteristic metabolic abnormalities. These syndromes consist of impaired management of sodium, potassium and chloride in the renal tubules. Underlying genetic abnormalities impair the kidney's ability to reabsorb electrolytes, leading to typical signs and symptoms of the condition.
15 genes analyzed
It is recommended if:
This report is ideal for patients with a clinical suspicion of Bartter and Gitelman Syndromes.
List of main conditions:
- Bartter syndrome, type 3
- Bartter syndrome, type 5, antenatal, transient
- Bartter 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.
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