Article type :

Case Report

Author :

Atul Kaushik, Vinod VC, Shailaja SR, Ruchi Saharan, Munish Kumar

Volume :

3

Issue :

2

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.