Scientists watch rare DNA disorders in action
NCT ID NCT05484570
First seen Nov 01, 2025 · Last updated May 20, 2026 · Updated 31 times
Summary
This study follows 40 people with rare DNA repair disorders like Cockayne syndrome, xeroderma pigmentosum, and trichothiodystrophy. Researchers will measure movement, balance, and other health changes over time to better understand how these conditions progress. No new treatments are being tested—the goal is to learn more about the diseases.
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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.
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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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Study contacts
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Contact
Email: •••••@•••••
Locations
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University of Minnesota- Twin Cities
RECRUITINGMinneapolis, Minnesota, 55455, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.