Rubinstain -taybi Syndrome: An Unusual Case Report

RUBINSTAIN -TAYBI SYNDROME is an unusual genetic disorder which affects many systems of the body, characterized by growth and developmental delays, distinctive craniofacial features & intellectual disability. A 12- year- old girl reported in the department of oral medicine and radiology with a chief complaint of decayed teeth. Patient was medically challenged. Extraoral features revealed distinctive cranio-facial appearance with broad thumbs and halluces and intraoral features observed were talon cusp in the maxillary central incisors, narrow maxillary arch, carious teeth and plaque accumulation. Considering the history, clinical characteristics and radiographic investigations, patient diagnosed as chronic irreversible pulpitis w.r.t 11.21.36.42,46. Chronic generalized marginal gingivitis with RUBINSTAIN -TAYBI SYNDROME type I. For effective management and good health of the patient, preventive and curative dental procedure and treatment plan had been taken. As an oral physician, understanding RUBINSTAIN -TAYBI SYNDROME is crucial because it requires a multidisciplinary approach to manage the oral health issues associated with it. Early intervention and continuous support are essential to maintaining the well-being of affected individuals.