*Address for Correspondence: Dr. Guru Prasad R., Professor Dept. of OMR People's College of Dental Science & Research Center, People's Campus, Bhanpur, Bhopal (M.P.)
The craniosynostosis syndromes constitute a group of conditions each haracterized by premature craniosynostosis occurring in association with a variety of other abnormalities. The most common of the craniosynostotic syndromes occurring without syndactyly is Craniofacial Dysostosis or Crouzon Syndrome. It is a genetic disease characterized by a variety of cranial deformities, facial malformations, eye changes and occasional other associated abnormalities1. Here we presented a case report of Crouzon Syndrome with review of Literature.
Craniosynostosis, Craniofacial Dysostosis, Crouzon syndrome
