Gene study aims to solve wolfram syndrome mystery
NCT ID NCT07485413
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at 45 people with certain changes in the WFS1 gene to figure out if they have a milder, dominant form of wolfram-like syndrome instead of the more severe recessive form. Researchers will use eye scans (OCT) to see if the gene changes are linked to specific eye problems. The goal is to better understand the disease, not to test a new treatment.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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HEGP
Paris, 75015, France
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Other studies related to the condition(s) this trial covers.
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