Dental Findings and Management in a Mucopolysaccharidosis Type IIIB Patient

J Dent Child (Chic). 2012 Sep-Dec;79(3):176-80.

Abstract

Mucopolysaccharidosis type IIIB (MPS IIIB) is an autosomal recessive disorder caused by deficiency of the lysosomal enzyme a-N-acetylglucosaminidase. Affected subjects present developmental delay, attention deficit disorder, uncontrollable hyperactivity, and aggressive behavior, followed by progressive dementia and death in late adolescence. The purpose of this paper is to report the dental findings and treatment in a child with MPS IIIB. His primary molars and permanent mandibular incisors presented obliterated pulp chambers and root canals, which may be a clinical manifestation of this disorder.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Dental Care for Persons with Disabilities
  • Dental Caries / diagnosis
  • Dental Caries / therapy
  • Dental Pulp Cavity / abnormalities
  • Dentigerous Cyst / diagnostic imaging
  • Follow-Up Studies
  • Humans
  • Incisor / abnormalities
  • Male
  • Mandibular Diseases / diagnostic imaging
  • Molar / abnormalities
  • Molar, Third / abnormalities
  • Mucopolysaccharidosis III / pathology*
  • Radiography
  • Tooth Diseases / diagnosis*
  • Tooth Diseases / therapy
  • Tooth Germ / abnormalities
  • Tooth, Deciduous / abnormalities