1Associate Professor, Department of Pediatrics, Sree Balaji Medical College and Hospital, Bharath Institute of Higher Education and Research, Chennai
2Professor & HOD, Department of Pediatrics, Sree Balaji Medical College and Hospital, Bharath Institute of Higher Education and Research, Chennai
*Corresponding author: Dr. Shanthi Ramesh, Associate Professor, Department of Pediatrics, Sree Balaji Medical College & Hospital, 7 Works Road, New Colony, Chromepet, Chennai-600 044, India. Mobile number: 9840938243, E mail: drshanthiramesh@gmail.com
Online published on 27 March, 2020.
Crouzon disorder was first detailed by a French neurosurgeon in the year 1912. Crouzon disorder is an uncommon hereditary issue. It is acquired as an autosomal predominant attribute. The sutures in the human skull meld after the total development of the cerebrum, however on the off chance that any of these sutures close rashly, it might then meddle with the development of the mind. Crouzon disorder is described by craniosynostosis, with related dentofacial oddities. This report depicts the different clinical and radiological highlights in a multi year old male kid, with specific reference to the trademark discoveries of this disorder.
Crouzon syndrome, craniosynostosis, brachycephaly
