Orofacial manifestations of Robinow syndrome: A rare case report

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Case Report

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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Abstract

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.

Keywords: 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

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