Child With Non-syndromic Lambdoid Craniosynostosis: A Rare Presentation

Yusuf Parvez *

Dubai Medical College for Girls, United Arab Emirates.

Samira Zoreik

Dubai Medical College for Girls, United Arab Emirates.

*Author to whom correspondence should be addressed.


Abstract

Nonsyndromic lambdoid craniosynostosis is a significantly rare type of craniosynostosis where one of the lambdoid sutures fuses prematurely. This craniofacial anomaly is most often diagnosed before the age of 12 months and therefore early treatment is important to prevent neurological dysfunction, developmental delay, further facial anomalies, as well as disturbances with the optic nerve therefore affecting the eyes. This is managed by performing a posterior open cranial vault reconstruction surgery as well as a lambdoid occipital reconstruction. We report a rare case of non syndromic right lambdoid craniosynostosis in a 19 months old girl.

Categories: Neurosurgery, Pediatrics, Neurology.

Keywords: Lambdoid craniosynostosis, non syndromic lambdoid craniosynostosis, craniofacial anomaly, lambdoid occipital reconstruction, posterior open cranial vault reconstruction


How to Cite

Parvez, Yusuf, and Samira Zoreik. 2024. “Child With Non-Syndromic Lambdoid Craniosynostosis: A Rare Presentation”. Asian Journal of Pediatric Research 14 (10):29-32. https://doi.org/10.9734/ajpr/2024/v14i10393.

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