01-02-2021 | Tarsorrhaphy | Case Report
Fronto-orbital advancement in a patient with Marshall-Smith syndrome: a case report and review of the literature
Published in: Child's Nervous System | Issue 2/2021
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Objective
The present report aimed to document the clinical features of a case of Marshall-Smith syndrome (MSS), an extremely rare embryonic developmental disorder with associated craniosynostosis.
Patient and method
We presented herein a case of a 2-year-old female patient with MSS who underwent fronto-orbital advancement for multisuture craniosynostosis.
Results
The patient’s proptosis improved after surgery, and no further surgical intervention was required for corneal exposure. A second FOA followed by revision tarsorrhaphy further improved eye closure.
Conclusion
Surgical procedures to correct dysplastic features and limit neurological impairment are a worthwhile supportive treatment for improving the quality of life and general condition of patients with MSS.