Eye scans help solve genetic mystery in rare wolfram cases
NCT ID NCT07485413
First seen Mar 22, 2026 · Last updated May 13, 2026 · Updated 8 times
Summary
This study looks at 45 people with certain gene changes to figure out if they have a milder, dominant form of wolfram-like syndrome instead of the usual recessive type. Researchers use eye scans to see how the retina is affected. The goal is to better understand these gene changes, not to test a new treatment.
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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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Locations
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HEGP
Paris, 75015, France
Conditions
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