Metopic and Sagittal Craniosynostosis in Williams Syndrome
- PMID: 37246286
- DOI: 10.1097/SCS.0000000000009394
Metopic and Sagittal Craniosynostosis in Williams Syndrome
Abstract
Craniosynostosis has been previously reported in patients with Williams syndrome. Due to the associated significant cardiovascular anomalies, with an attendant increased risk of death under anaesthesia, most patients have been managed conservatively. Here we report the multidisciplinary approach in a 12-month-old female infant with Williams syndrome who has metopic and sagittal craniosynostosis. The child successfully underwent calvarial remodelling procedures, with the clinical outcome demonstrating dramatically improved global development after surgery.
Copyright © 2023 by Mutaz B. Habal, MD.
Conflict of interest statement
The authors report no conflicts of interest.
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