Stickler syndrome

MONDO:0019354

Stickler syndrome is an inherited vitreoretinopathy characterized by the association of ocular signs with more or less complete forms of Pierre-Robin sequence, bone disorders, and sensorineural deafness (10% of cases).

Also known as: Stickler syndrome, hereditary progressive arthroophthalmopathy

17 clinical trials for this condition and its sub-types, 2 tagged with Stickler syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Syndromic disease (7133) ↑ Vitreoretinal degeneration (45) ↑ Spondyloepiphyseal dysplasia (8)

Sub-types of Stickler syndrome

Stickler syndrome type 1 3 trials
1 sub-type
- Stickler syndrome, type I, nonsyndromic ocular 0 trials
Stickler syndrome type 2 2 trials
Stickler syndrome, type 4 0 trials
Stickler syndrome, type 5 0 trials
Stickler syndrome, type 6 0 trials

Including sub-types (17) Tagged with Stickler syndrome (2)

Not yet finished but already full! 1 Completed 1

Eye surgery trial to prevent blindness in stickler syndrome pulled before start

Prevention Cancelled

This study aimed to see if a surgical procedure called scleral buckling could prevent retinal detachment in people with Stickler syndrome, a genetic condition that raises the risk of vision loss. The plan was to treat one eye in patients aged 5 to 35 who had already lost vision i…

Phase 2 • Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Prevention

Last updated Jun 27, 2026 12:29 UTC

Stickler syndrome

Where it sits in the disease tree

Eye surgery trial to prevent blindness in stickler syndrome pulled before start