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EP 17 Saquib Lakhani

EP 17 Saquib Lakhani

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 🔬 “From ICU to Genome: Dr. Saquib Lakhani on CRELD1, Early Detection & Rare Disease Advocacy” | Rare Awareness Radio 🎧 In this powerful episode of Rare Awareness Radio, we sit down with Dr. Saquib Lakhani, Director of the Early Detection Program at Cedars-Sinai Guerin Children’s and a leading pediatric critical care physician. Dr. Lakhani shares how a single ICU case launched a global collaboration that uncovered the link between CRELD1 and a new spectrum of rare genetic disorders involving seizures, developmental delay, and cardiac irregularities. We explore the diagnostic odyssey faced by families, the promise of genomic sequencing, the impact of early detection, and the inspiring role of patient communities like CRELD1 Warriors. 💡 Whether you're a researcher, clinician, advocate, or parent — this episode highlights how science, empathy, and global teamwork are transforming the future of rare disease care. 🧬 Topics covered: Understanding CRELD1 and its clinical implications The importance of early molecular diagnosis Collaborating across labs, hospitals, and continents Supporting families through the diagnostic journey The role of AI and emerging technologies in rare disease research 📍 Listen now and help us raise awareness — because every rare story deserves to be heard. #RareDisease #CRELD1 #Genomics #PediatricCare #EarlyDetection #RareAwarenessRadio #GeneticResearch #PatientAdvocacy #SaquibLakhani #CedarsSinai #PrecisionMedicine

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