Publications by authors named "Nimishabalakrishnan Vathariparambath"
Aim And Objective: The aim and objective of this report is to describe the dental management of 11-year-old patient with type III osteogenesis imperfecta (OI).
Background: Osteogenesis imperfecta or brittle bone disease is caused by mutations in the collegen type I gene which is a heterogeneous rare connective tissue disorder. Dentinogenesis imperfecta, hearing impairment, scoliosis, sclera is blue, hyperlaxity of ligaments, and fragile skin are other common features.