Cystic Fibrosis (CF) is a rare genetic condition that affects the lungs and digestive system, making early awareness and proper care essential. In this episode, we simplify the basics of...
In this episode of the Rare Info Series by Organization for Rare Diseases India (ORDI), we explore the fundamentals of genetic testing — what it is, why it matters, and...
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,...
Join us in this insightful episode where we explore the complex world of inborn errors of metabolism (IEM) in newborns—rare genetic disorders that can significantly affect a child’s health and...
In this episode of the Rare Info Series by ORDI (Organization for Rare Diseases India), we explore the often misunderstood world of immunodeficiency diseases. 🧬 Dr. Ankur Jindal, Senior Consultant...
Join us for a thought-provoking episode where we delve into the evolving landscape of genomics in India—its current status, ongoing advancements, and the promising road ahead. 🎙️ Speaker: Dr. Ashwin...
In Episode 17 of the RARE INFO SERIES, we dive into the essential aspects of rehabilitation for individuals living with Duchenne Muscular Dystrophy — a rare genetic disorder marked by...
In this episode, we explore how physiotherapy plays a crucial role in the management of Duchenne Muscular Dystrophy (DMD) — focusing on how functional ability testing is translated into effective...
In this insightful session, we delve into the devastating effects of Stevens Johnson Syndrome (SJS) — a rare but serious condition that can lead from painful burns to irreversible blindness....
Inherited Metabolic Disorders (IMDs) may be rare, but their impact is profound—especially in children. In this episode, we explore how small genetic changes can disrupt essential metabolic pathways, leading to...
