Patient enrollment enables us to:
- Identify the genetic variants responsible for VEO-IBD and define the molecular networks which are disrupted as a result of these variants.
- Create an innovative Pediatric VEO-IBD Portal for Personalized Patient Care (P4Care) to develop tailored treatments for VEO-IBD patients.
- Determine environmental factors affecting genetic and immunologic pathways relevant to VEO-IBD.