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Does Recessive Optic Atrophy Due to WFS1 Exist?
Sponsor: Hôpital Necker-Enfants Malades
Summary
All patients with Wolfram syndrome and recessive optic atrophy due to a mutation of the WFS1 from a single Center were included in a retrospective study. Evolution of the visual acuity since the occurrence of the optic atrophy and its last value, OCT data, genetic data and systemic manifestations were analyzed.
Official title: Does Recessive Optic Atrophy Due to WFS1 is a Specific Entity Different From Wolfram Syndrome?
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
45
Start Date
2026-02
Completion Date
2026-04
Last Updated
2026-01-13
Healthy Volunteers
No
Interventions
analyse study
Retrospective analyse and study of recorded data of patients with wolfram syndrome or recessive optic atrophy due to WFS1 mutation