+91 8617752708

Journal of Advances in Medicine and Medical Research, ISSN: 2456-8899, ISSN: 2231-0614 (Past),Vol.: 25, Issue.: 4

Case Report

Clinicoradiological Correlation of Crouzon Syndrome – A Case Report


P. Venkatalakshmi Aparna1, F. Massillamani1, A. Priyadharshini1* and D. K. S. Lakshminrusimhan

1Department of Oral Medicine and Radiology, Ragas Dental College and Hospital, Chennai, India.

Article Information


(1) Sandra Aparecida Marinho, Professor, Paraíba State University (Universidade Estadual da Paraíba - UEPB), Campus, Brazil.


(1) Ali Al Kaissi, Orthopedic Hospital of Speising, Austria.

(2) Dorina Lauritano, University of Milan-Bicocca, Italy.

(3) Mehmet Yaltirik, Istanbul Universty, Turkey.

Complete Peer review History:


Crouzon's syndrome is a rare autosomally dominant genetic disorder with complete penetrance and variable expressivity. In 1912 a French neurosurgeon first described this disorder. There is a mutation in the fibroblast growth factor receptor 2 (FGFR2) gene which causes this syndrome. Crouzon's syndrome is characterised by premature closure of sutures in the skull predominantly involving coronal and sagittal suture resulting in interference in the growth of the brain.   

Keywords :

Crouzon's syndrome; fibroblast growth factor; craniofacial synostosis; copper beat appearance.

Full Article - PDF    Page 1-5

DOI : 10.9734/JAMMR/2018/38904

Review History    Comments

Our Contacts

Guest House Road, Street no - 1/6,
Hooghly, West Bengal,

+91 8617752708


Third Floor, 207 Regent Street
London, W1B 3HH,

+44 20-3031-1429