ABOUT UAERDSC 2026
CONFERENCE OBJECTIVES
- To enhance awareness and understanding of rare diseases among healthcare professionals and the general public.
- To provide a platform for sharing the latest research, diagnostic, and therapeutic advancements in rare diseases.
- To facilitate networking and collaboration among stakeholders in the rare disease community.
- To promote patient advocacy and support for individuals and families affected by rare diseases.
- To discuss challenges and opportunities in rare disease diagnosis, treatment, and access to care in the UAE and the region.
- To educate healthcare providers on the importance of early diagnosis and appropriate management of rare diseases.
- To improve the quality of life for patients and families affected by rare diseases.
WHY ATTEND THE CONGRESS
(KEY POINTS)
- Gain insights into the latest advancements in rare disease research and treatment.
- Network with leading experts, researchers, and clinicians in the field.
- Learn about best practices in diagnosis, management, and care of rare disease patients.
- Connect with patient advocacy groups and families affected by rare diseases.
- Earn continuing medical education (CME) credits.
- Contribute to the growing awareness and understanding of rare diseases in the UAE & the region.
- Discover new opportunities for collaboration and research.
- Stay updated on the latest policies and initiatives related to rare diseases.
- Be part of a community dedicated to improving the lives of those affected by rare diseases.
TARGET AUDIENCE
- Geneticists
- General Pediatricians
- Pediatric sub-specialty
- Cardiologists
- Pulmonologists
- Endocrinologists
- Neonatologists
- Oncologists
- Hematologists
- Ophthalmologists
- ENT
- Dermatologists
- Neurologists
- Nephrologists
- Rheumatologists
- Anesthesiologists
- ENT specialist
- Family physicians
- Internalist
- Metabolic Consultants
- Psychiatrists
- Genetic Consolers
- Nurses
- Dieticians
- Metabolic Dieticians
- Physiotherapists
- Learning difficulties specialists
- Speech Therapists
- Academic scientists
- Researches
- Medical / Science students
- Laboratory technologist-Genetics
- Molecular geneticist
- Cytogenetic specialist
- Trainers
- Rare Heroes / Rare Families / Rare Caregivers.
- Community service providers
- POD service providers
- Non-Profit Organizations.
- Patients Advocacy Bodies.
- POD/Special Needs Business-Application Developers.
CONGRESS HIGHLIGHTS
- Genetics and Genomics of Rare Diseases
- Newborn Screening for Rare Disorders
- Diagnostic Approaches and Challenges
- Innovative Therapies and Clinical Trials
- Patient Advocacy and Support
- Ethical Considerations in Rare Disease Management
- Rare Disease Registries and Data Collection
- Specific Rare Disease Focus (e.g., metabolic disorders, neurological disorders, etc.)
- The role of Artificial Intelligence in Rare Diseases