PLCG2 - autoinflammation, antibody deficiency, and immune dysregulation syndrome
This test is available for the following conditions:
- Conditions > Immunological, hereditary > Autoinflammation, antibody deficiency, and immune dysregulation syndrome
This product is also part of the following panels:
- Mendelian inherited disorders panel with genome wide CNV analysis
- Metabolic disorders panel
- Primary immunodeficiencies panel
- Skin disorders panel¹
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
17966
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane