Evidence map›Paper›PMID 41768284›Full record

ArticleJPRAS open2026

Retinal detachment in patients with Sticklers syndrome: A comprehensive analysis for craniofacial surgeons.

Annelie J Bleeker, Nathaniel A T Sullivan, Anna H Brouwer, Elizabeth J de Koster, Michelle B van Egmond-Ebbeling, Elsbeth S M Voskuil-Kerkhof, Peter A W Schellekens, Marie-José H van den Boogaard, Corstiaan C Breugem

Abstract read
In one paragraph

Article in JPRAS open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Annelie J BleekerDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht, the Netherlands.
Nathaniel A T SullivanDepartment of Pediatric Plastic and Reconstructive Surgery, University Medical Center Amsterdam, Amsterdam, the Netherlands.
Anna H BrouwerDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht, the Netherlands.
Elizabeth J de KosterDepartment of Radiology and Nuclear Medicine, Radboud University Medical Centre, Nijmegen, the Netherlands.
Michelle B van Egmond-EbbelingDepartment of Ophthalmology, Eyescan, Ede, the Netherlands.
Elsbeth S M Voskuil-KerkhofDepartment of Ophthalmology, Eyescan, Ede, the Netherlands.
Peter A W SchellekensDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht, the Netherlands.
Marie-José H van den BoogaardDepartment of Clinical Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.
Corstiaan C BreugemDepartment of Pediatric Plastic and Reconstructive Surgery, University Medical Center Amsterdam, Amsterdam, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Stickler syndrome (SS) is the leading cause of hereditary retinal detachment (RD) in children and is characterized by ophthalmic, auditory, orofacial, and articular abnormalities. Vision loss often results from retinal events (RE), including retinal tears and detachments. Purpose: To identify clinical and genetic risk factors for retinal events in patients with SS, to guide screening and preventive care. Methods: This retrospective cohort study included 78 patients with clinically or genetically confirmed SS seen at the University Medical Center Utrecht between 2000 and 2019. Predictors included family history of SS, presence of a COL2A1 pathogenic variant, and degree of myopia. The primary outcome was occurrence of a retinal event, defined as a retinal tear or detachment confirmed by an ophthalmologist. Covariates were age, sex, Pierre Robin sequence, refractive error, retinopathy, hearing problems, joint problems, and cleft palate. Descriptive statistics, univariate analyses, and multivariate Kaplan-Meier survival models with multiple imputation and Firth's correction were used. Results: Nineteen of 78 patients (24%) developed at least one retinal event at a median age of 14 years. Multivariate analysis revealed that a positive family history of SS (HR 5.53, 95% CI 1.42-21.55), COL2A1 pathogenic variant (HR 3.59, 95% CI 1.00-12.82), and greater myopic refractive error (HR 0.86, 95% CI 0.74-0.99) were significantly associated with increased RE risk. Conclusion: A positive family history, COL2A1 mutation, and higher myopia independently predict retinal events in Stickler syndrome. Regular ophthalmologic screening is recommended for younger and high-risk patients, while education on early symptoms of retinal detachment is essential for older children and adults.

Indexed as

COL2A1Hereditary connective tissue disordersRetinal detachmentRisk factorsRobin sequenceStickler syndrome

Identifiers

PMID41768284
PMCPMC12936465

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.