Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

Users Online : 24041

Case report
Table of Contents - Year : 2016 | Month : March | Volume : 10 | Issue : 3 | Page : ZD09 - ZD10

Orofacial Manifestations of Autosomal Recessive Robinow’s Syndrome: A Rare Case Report ZD09-ZD10

Santosh Mali, Neha Bansal, Amol Dhokar, Monica Yadav

Dr. Bansal Neha,
H. No. 106, Sec 2B, Street No.4, Mandi Gobindgarh, Punjab-147301, India.
E-mail :

Robinow’s syndrome is a very rare genetic disorder which bears a resemblance to a foetal face. It is characterized by short-limbed dwarfism, defects in vertebral segmentation and abnormalities in the head, face and external genitalia. It has a genetic heterogeneity with autosomal dominant and recessive forms which relates to the severity of phenotype presentation. A rare case of an autosomal recessive form of Robinow’s syndrome is presented with emphasis on, characteristic craniofacial and intraoral manifestations to aid in diagnosis and dental management of this patient.