Visual outcomes in children with syndromic craniosynostosis: a review of 165 cases
- PMID: 33972704
- PMCID: PMC9046153
- DOI: 10.1038/s41433-021-01458-5
Visual outcomes in children with syndromic craniosynostosis: a review of 165 cases
Abstract
Objective: To determine visual outcomes and prevalence of amblyogenic risk factors in children with Apert, Crouzon, Pfeiffer and Saethre-Chotzen syndromes.
Methods: We conducted a single-centre, retrospective chart review of patients assessed at our unit between October 2000 and May 2017. Our outcome measures were as follows: age at first and last examination, refraction, horizontal ocular alignment, alphabet pattern deviations, anterior segment appearance, fundus examination findings, visual evoked potentials (VEPs) and genetics. The study's primary endpoint was the proportion of children achieving best-corrected visual acuity (BCVA) ≥ 6/12 in the better eye at final visit, as per UK driving standards.
Results: 165 patients were included in this study. Breakdown of diagnoses was as follows: Crouzon (n = 60), Apert (n = 57), Pfeiffer (n = 14) and Saethre-Chotzen (n = 34). 98 patients were male. Of 133 patients with full BCVA data available, 76.7% achieved BCVA ≥ 6/12 in the better eye. Of 122 patients, anisometropia >1.00 dioptre sphere (DS) affected 18.9% and astigmatism ≥1.00DS in at least one eye affected 67.2%. Of 246 eyes, 48.4% had oblique astigmatism. Of 165 patients, 60 had exotropia and 12 had esotropia. 48 of 99 patients demonstrated 'V' pattern. On multivariable logistic regression, nystagmus (p = 0.009) and ON involvement (p = 0.001) were associated with decreased vision in the worse eye. Normal VEPs were associated with better BCVA (p = 0.036).
Conclusion: There was a high prevalence of amblyogenic factors, however, the majority achieved BCVA ≥ 6/12 in their better eye. Optic neuropathy and nystagmus had the most significant impact on vision. VEPs can help the in overall assessment of visual function.
© 2021. The Author(s), under exclusive licence to The Royal College of Ophthalmologists.
Conflict of interest statement
The authors declares no competing interests.
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References
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- Cohen MM Jr. Apert, crouzon, and pfeiffer syndromes. In: Muenke M, Kress W, Collmann H, Solomon BD, editors. Monographs in human genetics. Basel: Karger; 2011. vol. 19, pp 67–88. 10.1159/isbn.978-3-8055-9595-7
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- Kressa W, Collmann H. Saethre-chotzen syndrome: clinical and molecular genetic aspects. In: Muenke M, Kress W, Collmann H, Solomon BD, editors. Monographs in human genetics. Basel: Karger; 2011. vol. 19, pp. 98–106. 10.1159/isbn.978-3-8055-9595-7
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- Muenke M, Kress W, Collman H, Solomon BD. Craniosynostoses: molecular genetics, principles of diagnosis, and treatment. Basel, Switzerland: S. Karger; 2011
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