Oral and dental manifestations in Rubinstein-Taybi syndrome: report of a rare case.

Rubinstein-Taybi syndrome, or broad thumb-hallux syndrome, is a well-defined rare congenital disorder characterised by postnatal growth deficiency, craniofacial dysmorphism, broad thumbs and great toes, and mental retardation (intellectual disability). Occurrence may be either sporadic or through autosomal dominant inheritance. Reports of Rubinstein-Taybi syndrome are scarce in the literature. This case report describes the oral and dentofacial findings of Rubinstein-Taybi syndrome affecting a 13-year-old Indian female, including the uncommon presence of talon cusps and an unerupted supernumerary tooth.

Fused double supernumerary premolars of the mandible: a rare case.

The incidence of nonsyndromic supernumerary premolars is rare. Supernumerary premolars are likely to undergo pathological changes. The most commonly encountered complications with these teeth are dentigerous cyst and root resorption of the adjacent tooth. This paper is about impacted double fused supernumerary premolars in the right mandiblular body associated with an impacted first premolar in a 17-year-old male. Under local anesthesia, the supernumerary premolars and the impacted permanent first premolar were surgically removed. Early diagnosis followed by an appropriate treatment at the right time will result in favorable prognosis in such cases.