Scientists investigate whether WFS1-related vision loss is a separate disease
NCT ID NCT07336966
First seen Jan 26, 2026 · Last updated May 19, 2026 · Updated 16 times
Summary
This study looks back at medical records of 45 people with WFS1 gene mutations to compare vision loss patterns between those with Wolfram syndrome and those with recessive optic atrophy alone. Researchers will analyze eye exams, genetic data, and other health information to see if these conditions are truly different. The goal is to better understand the disease, not to test a new treatment.
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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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Conditions
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