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Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II

Cited 78 time in Web of Science Cited 82 time in Scopus
Issue Date
2005
Publisher
Springer Verlag
Citation
AMERICAN JOURNAL OF HUMAN GENETICS (2005) 116: 186-191
Abstract
The current system for the classification of hereditary defects of tooth dentin is based upon clinical and radiographic findings and consists of two types of dentin dysplasia (DD) and three types of dentinogenesis imperfecta (DGI). However, whether DGI type III should be considered a distinct phenotype or a variation of DGI type II is debatable. In the 30 years since the classification system was first proposed, significant advances have been made regarding the genetic etiologies of inherited dentin defects. DGI type II is recognized as an autosomal dominant disorder with almost complete penetrance and a low frequency of de novo mutations. We have identified a mutation (c.52GT, p.V18F) at the first nucleotide of exon 3 of the DSPP (dentin sialophosphoprotein) gene in a Korean family (de novo) and a Caucasian family. This mutation has previously been reported as causing DGI type II in a Chinese family. These findings suggest that this mutation site represents a mutational hot spot in the DSPP gene. The clinical and radiographic features of these two families include the classic phenotypes associated with both DGI type II and type III. Finding that a single mutation causes both phenotypic patterns strongly supports the conclusion that DGI type II and DGI type III are not separate diseases but rather the phenotypic variation of a single disease. We propose a modification of the current classification system such that the designation hereditary opalescent dentin or DGI type II should be used to describe both the DGI type II and type III phenotypes.
ISSN
1432-1203
Language
English
URI
https://hdl.handle.net/10371/48039
DOI
https://doi.org/10.1007/s00439-004-1223-6
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College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Journal Papers (저널논문_치의학과)
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