Does Recessive Optic Atrophy Due to WFS1 Exist?

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Conditions studied: Wolfram Syndrome 1, Optic Atrophies, Hereditary

In brief

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.

Key facts

Study ID

NCT07336966

Run by

Hôpital Necker-Enfants Malades

People needed

45

Starts

2026-02-01

Expected to finish

2026-04-01

Last updated by the study team

2026-01-13

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• WFS1 mutation

You may not qualify if…

• WFS2 mutation

Full record on ClinicalTrials.gov

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