Understanding rare genetic conditions early can change the entire course of a child’s life. In this episode, we explore Prader–Willi Syndrome from birth through infancy, focusing on early signs, diagnosis, and care strategies. 🎙 Speaker: Dr. Bharathi Balachander Professor (Neonatal), St. John’s Medical College Hospital, Bengaluru 🎤 Moderator: Dr. Shweta Ramdas Scientist, Centre for Brain Research, Bengaluru 📌 Join us to learn from experts and support India’s rare disease community. 👉 Presented by ORDI – Organization for Rare Diseases India Together, we create awareness. Together, we bring hope. 💙 #ORDI #RareInfoSeries #RareDiseaseAwareness #PraderWilliSyndrome #NeonatalCare #InfantHealth #GeneticDisorders #SupportRareIndia
