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One Scientist's Bold Vision to Make on-Demand Treatments Routine for Life-Threatening Rare Genetic Diseases

Summary by Medical Xpress
In May 2025, researchers announced that K.J. Muldoon, a baby boy born without the ability to process dietary protein properly, had become the first person to be treated with a customized gene-editing therapy. Based on a technology developed by Broad Institute core member David Liu's laboratory, the treatment is the first in a series of new medicines being tested to treat rare diseases by repairing patients' particular genetic misspellings.

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Broad Institute broke the news in on Tuesday, June 24, 2025.
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