Gene hunt aims to solve rare skin disorder mysteries
NCT ID NCT02862834
First seen Mar 28, 2026 · Last updated May 22, 2026 · Updated 11 times
Summary
This study looked at 39 people with syndromic poikiloderma, a rare skin condition that also affects other parts of the body. Researchers used advanced genetic tests to find new genes that cause the disorder. The goal was to improve diagnosis, help families understand their genetic risks, and better monitor patients for tumors.
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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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Genom att skicka in godkänner du våra Användarvillkor
Locations
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CHU Dijon Bourgogne
Dijon, 21079, France
Conditions
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