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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

Online ISSN : 2581-3838

Print ISSN : 2581-382X

Article First Page : 74

Article End Page : 76


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