KJ Muldoon
KJ Muldoon is an infant who was recently in the news for being the first baby to receive a personalized gene-editing treatment for CPS1 deficiency, a rare genetic disorder that poses severe health risks.
Born on Jan 01, 2022 (3 years old)
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Each country's color is based on "Mentions" from the table above.
Recent Mentions
Croatia:
KJ Muldoon is the first person to undergo CRISPR therapy designed to correct his specific genetic mutation.
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Monaco:
KJ Muldoon is a 9-month-old baby diagnosed with a rare metabolic disorder called CPS1.
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Slovenia:
KJ Muldoon is a child who was treated with personalized gene therapy for a severe genetic disorder shortly after birth.
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Ireland:
KJ Muldoon became the first patient to receive a custom gene-editing treatment for CPS1 deficiency.
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Portugal:
KJ Muldoon is a baby who was diagnosed with a rare disease that may require gene editing for treatment.
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Hong Kong:
KJ Muldoon was diagnosed with a rare genetic disorder shortly after birth.
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Dominican Republic:
KJ Muldoon is a baby diagnosed with a rare genetic disorder who received experimental gene editing treatment.
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Mexico:
KJ is a baby who was born with a rare disease that typically results in death within a week.
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United States:
KJ Muldoon is a baby born with a rare and dangerous genetic disease who is growing and thriving after getting an experimental gene editing treatment made just for him.
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United States:
KJ Muldoon is the baby diagnosed with CPS1 deficiency.
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