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Dental Findings and Management in a Mucopolysaccharidosis Type IIIB Patient

Authors :
Talitha de Siqueira, Mellara
Danielle Torres, Azevedo
Gisele, Faria
Paulo, Nelson Filho
Alexandra Mussolino de, Queiroz
Luiz Guilherme, Brentegani
Source :
Journal of dentistry for children (Chicago, Ill.). 79(3)
Publication Year :
2013

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.

Details

ISSN :
19355068
Volume :
79
Issue :
3
Database :
OpenAIRE
Journal :
Journal of dentistry for children (Chicago, Ill.)
Accession number :
edsair.pmid..........5c77a1355678d82ec772e609bab5efff