A Case Report on Apert Syndrome
DOI:
https://doi.org/10.3329/jmj.v20i2.79464Keywords:
Apert syndrome, Craniosynostosis, SyndactylyAbstract
Apert syndrome (Acrocephalosyndactyly) is a rare congenital disorder characterised by craniosynostosis, midfacial malformation, and symmetric syndactyly of the hands and feet. The prodromal characteristics for the typical cranio-facial appearance are early craniosynostosis of the coronal suture, cranial base, and agenesis of the sagittal suture. The reporting case presented with several cranio-facial deformities, including brachycephaly, midface hypoplasia, flat face, hypertelorism, ocular proptosis, down-slanting palpebral fissures, and syndactyly with osseous fusion of the hands and feet. Intraoral findings included a high arched palate with pseudocleft in the posterior one-third.
Jalalabad Med J 2023; 20 (2): 72-75
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