Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders
NCT ID NCT07535372
First seen Apr 20, 2026 · Last updated May 25, 2026 · Updated 8 times
Summary
This early-stage study aims to develop a personalized treatment for children with syndromic craniosynostosis, a group of rare genetic disorders where skull bones fuse too early. The approach uses a nano-engineered gel to deliver custom genetic medicine directly to the affected area, potentially reducing the need for repeated surgeries. The study involves 12 children aged 0-5 years and will first test the treatment in lab-grown cells and mouse models.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Institut Imagine
Paris, France
Conditions
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