Congenital Neutropenia Report
Congenital Neutropenia
Congenital neutropenia is a rare genetic disorder characterized by a decreased number of neutrophils, a type of white blood cell that helps fight infections. This can lead to recurrent infections, inflammation, and other complications. Congenital neutropenia is caused by mutations in several different genes that play a role in the production and function of neutrophils. This report tests for genetic variants in these genes to help diagnose congenital neutropenia and guide treatment decisions.
More than 25 genes analyzed
It is recommended if:
This report is designed for individuals with symptoms of neutropenia or a family history of the condition. Genetic testing can confirm a diagnosis, identify the specific genetic variant responsible for the condition, and help guide treatment decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
List of main conditions:
- Congenital neutropenia
- Cyclic neutropenia
- Severe congenital neutropenia
Simple workflow
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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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