Rare Bone Disease
Educational Symposium
CME Accredited scientific symposium focused on rare genetic bone disorders, diagnostic approaches, multidisciplinary collaboration, and recent advances in management.
Welcome Note
The Kuwait Academy of Rare Disease (KARD), in collaboration with the Kuwait Pediatric Association, is pleased to welcome you to the “Rare Bone Disease Educational Symposium” (CME Accredited).
This scientific symposium will focus on rare genetic bone disorders, providing a comprehensive overview of their classification, pathophysiology, and diagnostic approaches, along with in-depth discussions on key conditions such as Osteogenesis Imperfecta (OI), X-linked Hypophosphatemia (XLH), Hypophosphatasia (HPP), and skeletal dysplasia in MPS IVA & VI.
The program will also highlight recent advances in management and treatment strategies, aiming to improve patient outcomes and quality of life.
The agenda features expert-led presentations and interactive panel discussions, fostering multidisciplinary collaboration and practical clinical insights in the diagnosis and management of rare bone diseases.
The target audience includes pediatricians, pediatric endocrinologists, metabolic specialists, geneticists, orthopedic specialists, internists, allied healthcare professionals, and researchers involved in the care of patients with rare bone and metabolic disorders.
AGENDA
Advances in XLH Management
Diagnosis & Treatment of MPS IVA & VI