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.
Keyword :
Fetal facies, Brachymelia, Genetic disorder, Multidisciplinary management