About on Baby Treated With Genetic Editing Therapy For First Time Shorts
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Baby with rare disorder treated with breakthrough gene-editing therapy
Gene editing saves baby with rare genetic disease
Baby becomes world's first patient to receive personalised gene-editing treatment
Breakthrough in gene-editing therapy helps baby with rare disorder
Breakthrough gene editing treatment helps child born with rare disorder
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Last Updated: October 3, 2026
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Summary
Diagnosed with CPS1 deficiency, a rare urea cycle disorder, KJ was successfully One week after he was born, KJ Muldoon was diagnosed with what doctors call a CPS-1 deficiency, essentially meaning he was ... Doctors announced this week that they have
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