Complete Information on Dentinogenesis imperfecta with Treatment and Prevention
Genetic mutations, or alterations in an individual’s genome, can be inherited, affecting cells that perpetually divide (germ-line mutations), or they can occur at any point during a person’s life.
Dentinogenesis imperfecta is a disorder of tooth growth. This circumstance is inherited in an autosomal predominant form, which means one transcript of the altered gene in each cubicle is adequate to induce the disorder. There are three types of dentinogenesis imperfecta. Type I is associated with osteogenesis imperfecta. Type II was previously found to be linked to altered glycosaminoglycan concentrations. Type III is the brandywine form, named for the city brandywine, maryland, where there was a large population of patients with this disorder. Type III tends to be less severe than type II. The severity of discoloration and enamel fracturing in all dentinogenesis imperfecta types is highly variable even within the same family.
