Clinical and genetic analysis of a pedigree affected with hereditary dentinogenesis imperfecta type II.
10.3760/cma.j.cn511374-20211014-00811
- VernacularTitle:一个遗传性牙本质发育不全Ⅱ型家系的临床及遗传学分析
- Author:
Feiyang WANG
1
;
Ningxiang WANG
;
Tian ZHAO
;
Mei ZHANG
;
Wenlei WU
;
Weibin SUN
;
Juan WU
Author Information
1. Department of Periodontology, Nanjing Stomatological Hospital, the Affiliated Stomatological Hospital of Nanjing University Medical School, Nanjing, Jiangsu 210008, China. juanwu@smail.nju.edu.cn.
- Publication Type:Journal Article
- MeSH:
Dentinogenesis Imperfecta/genetics*;
Extracellular Matrix Proteins/genetics*;
Humans;
Mutation;
Pedigree;
Phosphoproteins/genetics*;
Sialoglycoproteins/genetics*
- From:
Chinese Journal of Medical Genetics
2022;39(9):1016-1020
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the clinical and genetic characteristics of a Chinese pedigree affected with hereditary dentinogenesis imperfecta (DGI) type II.
METHODS:Clinical data of the pedigree members were collected. Genomic DNA was extracted from peripheral blood samples and subjected to whole exome sequencing.
RESULTS:Clinical characteristics of the affected family members have included amber teeth along with significant attrition, constricted roots and dentine hypertrophy leading to pulpal obliteration, which were suggestive of DGI type II. All of the affected members were found to have harbored a novel heterozygous c.2837delA (p.Asp946Valfs*368) variant of the DSPP gene which was predicted to be likely pathogenic.
CONCLUSION:The c.2837delA variant of the DSPP gene probably underlay the disease in this pedigree. Above finding has expanded the variant spectrum of DSPP gene and provided a basis for molecular diagnosis and genetic counseling for this pedigree.
