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Orofacial manifestations of Robinow syndrome: A rare case report

Journal: IP International Journal of Maxillofacial Imaging (IJMI) (Vol.3, No. 2)

Publication Date:

Authors : ; ; ; ; ;

Page : 74-76

Keywords : Fetal facies; Brachymelia; Genetic disorder; Multidisciplinary management;

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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.

Last modified: 2017-07-13 19:29:07