DEFINING CHARACTERISTICS OF PRIMARY DENTITION IN A CHILD WITH ISOLATED PIERRE-ROBIN SEQUENCE: UNVEILING A NOVEL PHENOTYPIC EXPRESSION- A CASE REPORT

The Pierre Robin sequence (PRS), initially identified in 1923, is a congenital condition defined by a triad of features: micrognathia, glossoptosis, and cleft palate (CP).¹ The occurrence of PRS is estimated to be between 1 in 8,500 and 1 in 30,000 live births.² This article explores a unique phenotypic expression of primary dentition in a child diagnosed with Pierre-Robin sequence.