A Rare Case of Crouzon Syndrome
G. Ramya Balaprabha, Gandamala Jhansi Rani, Addula Meenakshi, Aliyangattuvageri Rajeez & Tadikonda Ramarao · International Journal of Medical and Pharmaceutical Case Reports · 2025
Background: Crouzon’s syndrome is a rare autosomal dominant genetic disorder caused by mutations in the FGFR2 gene. It leads to craniosynostosis, where the premature fusion of skull bones results in distinct craniofacial abnormalities. Key clinical features include towering skull...
Open access
Research Article
10.9734/ijmpcr/2025/v18i3432