Mutation analysis of a Chinese family with genetic dentinogenesis imperfecta.
- Author:
Er-jun QU
1
;
Hong-bo ZHANG
;
Lan-ying CHEN
;
Ling-biao GU
Author Information
- Publication Type:Journal Article
- MeSH: Amino Acid Sequence; Asian Continental Ancestry Group; genetics; Base Sequence; Dentinogenesis Imperfecta; genetics; Exons; Extracellular Matrix Proteins; genetics; Female; Humans; Male; Microsatellite Repeats; Molecular Sequence Data; Mutation; Pedigree; Phosphoproteins; Sialoglycoproteins; Young Adult
- From: Chinese Journal of Medical Genetics 2009;26(5):536-538
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the genetic etiology of an autosomal dominant dentinogenesis imperfecta in a Chinese family.
METHODSThe molecular change of the disease in the family was analyzed through the clinical examination, linkage analysis, mutational screening of the DSPP gene and restriction fragment length polymorphism analysis.
RESULTSThe disease related gene was completely linked with microsatellite marker D4S1534. We found a novel mutation in the first exon of the DSPP gene (c.49C>T, p.Pro17Ser). All patients in the family had the mutation, while this mutation was not observed in the normal individuals of this family and 100 unrelated controls.
CONCLUSIONThe p.Pro17Ser identified in the family was a new pathogenic mutation. Our finding provided further understanding of the molecular mechanism of dentinogenesis imperfecta.
