It is a congenital disorder of tooth development caused by the mutations in the AMELX, ENAM, MMP20, KLK-4, FAM83H, WDR72, LAMB3 and ITGB6 genes.
These genes encode for the proteins ameloblastin, enamelin, tuftelin and amelogenin that are responsible for the development and maintenance of the enamel.
Symptoms :
Discolored, unusually small, pitted or grooved teeth