Chronic Granulomatous Disease Panel
Chronic Granulomatous Disease Panel
Impossible de charger la disponibilité du service de retrait
The mutations underlying the Chronic Granulomatous Disease afflict the innate immunity, in particular the phagocytic function of macrophages, eosinophils, neutrophils and monocytes, which will no longer be able to destroy pathogenic organisms such as bacteria and fungi. This condition, therefore, leads to a high susceptibility to infections, the formation of granulomas and other inflammatory conditions affecting various tissues.
For those who experience the symptoms of Chronic Granulomatous Disease (recurring bacterial and fungal infections, with the formation of granulomas mostly in the lungs, gastrointestinal, liver and lymph nodes); for family planning purpose (in case disease-genes are known) and for family history for this condition.
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 8 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Granulomatous Disease, Chronic, Autosomal Recessive
- Granulomatous Disease, Chronic, X-Linked
- Hermansky-Pudlak Syndrome

Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.