The Life-Saving Secrets in Your Baby’s DNA | Robert C. Green | TED

The Life-Saving Secrets in Your Baby’s DNA | Robert C. Green | TED

October 05, 2025 11 min
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🤖 AI Summary

Overview

This talk explores the groundbreaking field of newborn genomic sequencing, highlighting its potential to predict and prevent treatable genetic conditions from birth. Robert C. Green shares insights from the BabySeq Project, the first clinical trial of newborn DNA sequencing, and discusses its implications for medicine, privacy, and the future of healthcare.

Notable Quotes

- If we really want to invent the future, we’ve got to realize that a child’s DNA doesn’t change over time, but the science is changing all the time.Robert C. Green, on the importance of revisiting genomic data as science advances.

- Finding out that your newborn has a heart problem is absolutely terrifying. But knowing we could be proactive gave us peace of mind.Mother 1, reflecting on the benefits of early genetic insights.

- I had risk-reducing and ultimately life-saving surgery, and I believe it was the right decision so I could be present for my son.Mother 3, on discovering her BRCA2 mutation through her child’s genomic sequencing.

🧬 The Promise of Newborn Genomic Sequencing

- BabySeq Project was the first clinical trial to sequence and analyze the genomes of healthy newborns, aiming to identify treatable genetic conditions early.

- Robert C. Green emphasized the tragedy of delayed diagnoses in children, which can lead to permanent damage despite the availability of treatments.

- Sequencing revealed that 4% of babies carried mutations linked to treatable conditions, while 12% had mutations associated with future risks, underscoring the prevalence of genetic vulnerabilities.

👶 Real-Life Impact Stories

- Baby Adam’s elastin gene mutation led to early detection of a narrowed aorta, enabling proactive monitoring and treatment.

- Baby Cora’s biotinidase deficiency was managed with a simple daily vitamin, preventing brain development issues.

- Baby Jacob’s BRCA2 mutation revealed a hereditary cancer risk, prompting his mother to undergo life-saving preventive surgery.

🔒 Privacy and Ethical Concerns

- Robert C. Green addressed fears around genomic privacy, noting that DNA data in medical contexts is protected similarly to psychiatric or HIV records.

- He contrasted medical-grade sequencing with direct-to-consumer genetic testing, which lacks the same legal protections and uses less precise genotyping technology.

- Resistance to newborn sequencing is partly psychological—parents hesitate to seek out potential problems in seemingly healthy babies.

🌍 Building a Global Genomic Future

- Green co-founded an international consortium of 27 groups working on newborn sequencing across diverse healthcare systems.

- He advocates for revisiting genomic data over time as science evolves, enabling continuous updates on risks and treatments.

- The vision includes scaling genome-informed medicine through AI-enhanced digital health platforms, aiming to save millions of lives and shift healthcare from reactive to preventive.

AI-generated content may not be accurate or complete and should not be relied upon as a sole source of truth.

📋 Video Description

What if we could get a heads-up about serious health issues before they begin, from the moment a baby is born? In this groundbreaking talk, geneticist and physician Robert C. Green shares how his team became the first in the world to comprehensively sequence and analyze the DNA of healthy newborns, revealing hidden risks for treatable conditions. The future of medicine isn’t just about curing illness, he says — it's about predicting and preventing it. (Recorded at TED2025 on April 10, 2025)

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