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A Novel Mutation in the DSPP Gene Associated with Dentinogenesis Imperfecta Type II

Cited 39 time in Web of Science Cited 38 time in Scopus
Authors
Lee, S.-K.; Lee, K.-E.; Jeon, D.; Lee, G.; Lee, H.; Shin, C.-U.; Jung, Y.-J.; Lee, S.-H.; Hahn, S.-H.; Kim, J.-W.
Issue Date
2009
Publisher
American and International Associations for Dental
Citation
J Dent Research, 88(1):51-55
Keywords
dentin sialophosphoproteinDSPPdentinogenesis imperfectadentin dysplasiasplicing assay
Abstract
Hereditary dentin defects are divided into dentinogenesis imperfecta and dentin dysplasia. We identified a family segregating severe dentinogenesis imperfecta. The kindred spanned four generations and showed an autosomal-dominant pattern of inheritance. The proband was a child presenting with a severely affected primary dentition, with wide-open pulp chambers and multiple pulp exposures, resembling a DGI type III (DGI-III) pattern. We hypothesized that a mutation in the DSPP gene is responsible for this severe phenotype. Mutational analyses revealed a novel mutation (c.53T>A, p.V18D) near the intron-exon boundary in the third exon of the DSPP gene. We analyzed the effect of the mutation by means of an in vitro splicing assay, which revealed that the mutation did not affect pre-mRNA splicing. Further studies are needed for a better understanding of the nature of the disease and the development of an appropriate treatment strategy.
ISSN
0022-0345
Language
English
URI
https://hdl.handle.net/10371/62256
DOI
https://doi.org/10.1177/0022034508328168
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College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Journal Papers (저널논문_치의학과)
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