Shortening the Diagnostic Journey: Genomics for Every Child – Tomorrow’s Cure Season 4 Episode 6
When a baby is critically sick and solutions are elusive, every single day can really feel like an eternity. This week on Tomorrow’s Cure from Mayo Clinic, host Cathy Wurzer talks with pediatric geneticist Whitney Thompson, M.D., from Mayo Clinic, genomic drugs pioneer Stephen Kingsmore, M.D., DSc, from Rady Children’s Institute for Genomic Medicine, and Sean George, Ph.D., CEO of Inflection Medicine, about how fast entire genome sequencing is remodeling look after the youngest sufferers.
Together, they discover how clinicians are shortening the “diagnostic odyssey,” pairing sequencing with synthetic intelligence to establish potential therapies, and redefining what is feasible for uncommon ailments by means of applications like Mayo Clinic Children’s BabyFORce. You will even hear highly effective affected person tales, together with kids whose lives modified after a genomic analysis opened the door to focused therapies, and a candid dialogue about price, entry, and ethics as this know-how strikes towards wider adoption. Tune in to learn the way immediately’s breakthroughs in pediatric genomics may form the way forward for drugs for all of us.
Visit https://tomorrowscure.com for extra info.
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0:00 Introduction and Why Rapid Genome Sequencing Matters
1:33 Understanding the Diagnostic Odyssey
3:18 How Whole Genome Sequencing Changed Care
5:19 Making Genomics Accessible Beyond Major Centers
7:19 What Sequencing Reveals About Rare Disorders
10:15 How AI Accelerates Genomic Interpretation
11:21 Baby Jorie: Personalized Treatment Breakthrough
16:39 Gene‑Targeted Therapies and N‑of‑One Medicine
21:29 Expanding Access Through State and Global Programs
25:31 Scaling Genomics and Therapies for All Patients
28:49 Why Experts Are Optimistic About the Future
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