Fanconi Anemia Report
Fanconi Anemia
Fanconi anemia is a rare inherited disorder that affects bone marrow function and increases the risk of developing certain types of cancer, such as leukemia. Fanconi anemia is caused by mutations in genes involved in DNA repair and cell cycle regulation.
More than 20 genes analyzed
It is recommended if:
This report is designed for individuals with a family history of Fanconi anemia or individuals with symptoms of the condition, such as abnormal blood counts or birth defects. 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:
- Fanconi Anemia
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.
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*Raw data will be available free of charge for the first 30 days after release.
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