Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III.

[dentin dysplasia]

A rare compound mutation involving a 36 bp deletion and 18 bp insertion within exon 5 of the dentin sialophosphoprotein (DSPP ) gene has been identified in a family with dentinogenesis imperfecta type III (DGI -III ). The DSPP gene encodes two major tooth matrix proteins dentin sialoprotein (DSP ) and dentin phosphoprotein (DPP ). DSPP mutations associated with DGI -III results in an in frame truncation of the serine aspartic acid triplet repeat found in DPP near the highly conserved carboxyl terminal region shortening the protein by six amino acids . Clinically this family presents with discolored amber opalescent teeth and severe attrition of the tooth structure . This study is the first report of a mutation within DPP associated with a genetic dentin disease . Our study indicates that DGI -III is allelic with some forms of DGI -II with and without progressive hearing loss and dentin dysplasia type II that have been shown to be caused by mutations within the DSP coding or signal peptide regions .

Diseases
Validation

Diseases presenting "progressive hearing loss" symptom

dentin dysplasia

pendred syndrome

This symptom has already been validated