The Journal of Dental Panacea
Official Publication of Dental Panacea
Official Publication of Dental Panacea
Online ISSN: 2348-8727
CODEN : JDP
The Journal of Dental Panacea (JDP) open access, peer-reviewed quarterly journal, Publish quarterly as Open Access (OA). Vision of this journal for better dissemination of knowledge, Journal will be publishing the article ‘Ahead of Print’ immediately on acceptance. In addition, the journal would allow free access (Open Access) to its contents, which is likely to attract more readers and citations to articles published in JDP. Manuscripts must be prepared in accordance with “Uniform requirements” of the The Journal of Dental Panacea as more...Case Report
Author Details :
Volume : 6, Issue : 2, Year : 2024
Article Page : 110-112
https://doi.org/10.18231/j.jdp.2024.022
Abstract
The autosomal dominant trait that causes Crouzon syndrome is inherited. A rare genetic disorder called Crouzon syndrome may show symptoms at birth or in early childhood. In most infants with Crouzon syndrome, the fibrous connection between some of the skull bones closes early. Trigonocephaly, scaphocephaly and brachecephaly are the consequences of premature closure. In certain cases, the disease does not run in the family of those affected.
Keywords: Crouzon syndrome, Craniosynostosis, Hypertelorism
How to cite : Roshna Ks, Shaji R T, Johny J, Sreedhar S, Vani Mh, Sailakshmi A, Crouzon syndrome - Acase report. J Dent Panacea 2024;6(2):110-112
This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution 4.0 International License, which allows others to remix, and build upon the work, the licensor cannot revoke these freedoms as long as you follow the license terms.
