Crouzon syndrome in an infant: a rare case report
Abstract Crouzon syndrome is a rare craniosynostosis syndrome, accounting for approximately 4.5% of cases, and is most often caused by pathogenic variants in the FGFR2 gene. We report the case of a 7-month-old male infant presenting with abnormal cranial shape since birth, progressive proptosis, and developmental delay.
Authors
- Rakshitha Prasad
- Ghouseya Begam
- Mithila Das Mazumder
- Divyasree Chimata
- Azmathulla Khan
Institutions
- Institute of Medical Sciences (IN)
Publication Details
- Journal
- MGM Journal of Medical Sciences
- Published
- 2025-10-01
- DOI
- https://doi.org/10.4103/mgmj.mgmj_259_25
- Primary Topic
- Craniofacial Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00