Orofacial manifestations of Robinow syndrome: A rare case report
Journal: IP International Journal of Maxillofacial Imaging (IJMI) (Vol.3, No. 2)Publication Date: 2017-06-01
Authors : Atul Kaushik; Vinod VC; Shailaja SR; Ruchi Saharan; Munish Kumar.;
Page : 74-76
Keywords : Fetal facies; Brachymelia; Genetic disorder; Multidisciplinary management;
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.
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Last modified: 2017-07-13 19:29:07