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IP International Journal of Maxillofacial Imaging

Orofacial manifestations of Robinow syndrome: A rare case report

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Author Details : Atul Kaushik, Vinod VC, Shailaja SR, Ruchi Saharan, Munish Kumar

Volume : 3, Issue : 2, Year : 2017

Article Page : 74-76

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Robinow syndrome (Online Mendelian Inheritance in Man, OMIM - 268310) is an extremely rare genetic disorder with characteristic skeletal deformities and orofacial dysmorphism (fetal facies). The purpose of the present case report is to highlight the orofacial manifestations in a pediatric patient which can facilitate the general practitioners in the early diagnosis and multidisciplinary dental and medical management of the syndrome.

Fetal facies, Brachymelia, Genetic disorder, Multidisciplinary management

How to cite : Kaushik A, Vinod Vc, Shailaja Sr, Saharan R, Kumar M, Orofacial manifestations of Robinow syndrome: A rare case report. IP Int J Maxillofac Imaging 2017;3(2):74-76

Copyright © 2017 by author(s) and IP Int J Maxillofac Imaging. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (