Congenital Neutropenia Panel


Whole Genome Sequencing 30X

This product is only meant for customers who already purchased a Dante Genome Test

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 panel tests for genetic variants in these genes to help diagnose congenital neutropenia and guide treatment decisions.
This panel 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.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.

  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • More than 25 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Congenital neutropenia
  • Cyclic neutropenia
  • Severe congenital neutropenia

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