Hurler syndrome: Oral and radiographic findings of a rare clinical case

Abstract

Hurler syndrome (HS) is a rare disorder which belongs to the category of mucopolysaccharidosis (MPS) caused due to inherited deficiencies of lysosomal α-L-iduronidase activity. Individuals with HS share specific facial features with several oral manifestations. We present through this article a case of a 15-year-old girl that was referred to the pediatric dentistry department at the center of dental consultation and treatment of Rabat, diagnosed with Hurler- syndrome with numerous oral manifestations.