Unlock Breakthroughs in Pediatric Care,
Empowering You to Transform
The Lives of Children with rare consitions !
About the Conference
About the Conference
The 1st National Conference on Rare Diseases in Children is a unique event that aims to bring together leading experts, healthcare professionals, researchers, policymakers, patient advocates, and families to address the care of children with rare diseases. Rare diseases, though individually uncommon, collectively affect millions of lives globally, demanding collaborative approaches for effective diagnosis, care, and treatment.
This conference seeks to bridge the gap by fostering collaboration, sharing ground-breaking research, and discussing innovative solutions to improve outcomes for children with rare diseases.
Who should attend
- Practicing Pediatricians & Pediatric Surgeons
- Clinical Geneticists
- Fetal Medicine Specialists
- Obstetricians
- Trainee Doctors
- Trainee and Researchers in Pediatric Rare Diseases
- Laboratory Professionals
- Metabolic Dieticians
- Rare Disease Advocates and Patient Groups
- Biotech and Pharma Professionals
- Policymakers and Public Health Officials
Key Highlights
5 Workshops
Hands-on, interactive learning experiences designed to help participants enhance their skills and explore new horizons.
Panel Discussions
Led by stalwarts in the field, exploring diagnosis, treatment strategies, innovative solutions and recent advances.
Keynote Address
Insights from leading authority in pediatric rare diseases.
Parent Support Group
Real-life perspectives offering inspiration and awareness.
Networking Opportunities
Build collaborations with advocates, policymakers, and industry professionals
Exhibition Booths
Showcasing advancements in therapies, research tools, and pediatric rare disease resources.
Hurry!!! Secure your spot today
Call for Abstracts
Submit your abstracts to careforrare@wadiahospitals.org
Abstract Submission Deadline: 31st January 2025
Become a Sponsor
We look forward to your participation in this unique conference held for the first time in India with respect to children with rare diseases.
