@article{Díaz_Hernández_2017, title={Crouzon’s Syndrome: Review of the literature and case report}, volume={24}, url={https://estomatologia.univalle.edu.co/index.php/revista_estomatologia/article/view/5799}, DOI={10.25100/re.v24i2.5799}, abstractNote={<p>Crouzon’s Syndrome: Congenital craniosynostosis characterised by the premature in-utero closure of the coronal, sagittal, and lambdoid sutures. It produces an abnormal growth of the cranium, hypoplasia of the jaw, and facial asimmetry. The case of a five year old girl with Crouzon Syndrome is presented; she consulted the service of Paediatric Dentistry at School of Dentistry of Universidad del Valle (Cali,Colombia). </p> <p>This work highlights the multidisciplinary approach and the orthopaedic pre-surgical management performed, it involved an intraoral fixed device for controlled expansion with a Hyrax type screw and a facial mask for maxillary protraction as treatment before surgery. The surgery was performed in mono-block and advancement with an osteogenic distactor was done.</p> <p><strong>Key words:</strong> Crouzon syndrome, craniosynostosis, proptosis, facial Asymmetry</p>}, number={2}, journal={Revista Estomatología}, author={Díaz, Paola-Andrea and Hernández, Jesús-Alberto}, year={2017}, month={Sep.} }