In this episode of ORDI’s Rare Info Series, we explore Osteogenesis Imperfecta (OI) — a rare genetic disorder also known as brittle bone disease. Learn about the clinical features, diagnosis, and the latest approaches to management from leading experts in medical genetics. Speaker: Dr. Prajnya Ranganath (MD Paediatrics, DM Medical Genetics) Professor, Department of Medical Genetics, Nizam’s Institute of Medical Sciences (NIMS), Hyderabad. Moderator: Dr. Kshitija Patil (MBBS, MD Paediatrics, DM Medical Genetics – AIIMS, New Delhi) Fellowship Clinical Genetics (MUHS), Consultant Clinical Geneticist, Apollo Hospitals, Navi Mumbai. 📌 About ORDI: Organization for Rare Diseases India (ORDI) is dedicated to improving the lives of people affected by rare diseases through awareness, advocacy, and research. #OsteogenesisImperfecta #RareDiseases #MedicalGenetics #ORDI #RareInfoSeries #BrittleBoneDisease #GeneticDisorders #PatientAwareness
