Gulati, NikitaJuneja, SaurabhSingh, AkritiSingh, Iqbal2020-01-022020-01-022019-07Gulati Nikita, Juneja Saurabh, Singh Akriti, Singh Iqbal. A histological continuum between dentinogenesis imperfecta and dentin dysplasia: A case report with literature review. Indian Journal of Dental Research. 2019 Jul; 30(4): 643-6460970-92901998-3603http://imsear.searo.who.int/handle/123456789/192292Dentinogenesis Imperfecta and dentin dysplasia are genetic oral diseases inherited in a simple autosomal dominant mode, with high penetrance and a low mutation rate. Both of them are present with bulbous crowns, marked cervical constrictions, severe attritions, few periapical radiolucencies, and premature tooth loss. The diagnosis is based on family history, and detailed clinical examination, while genetic diagnosis may become useful in the future once sufficient disease-causing mutations have been discovered. Here, we present a case with overlapping features of both dentinogenesis imperfecta and dentin dysplasia asserting both the anomalies to be part of the same continuum of the genetic event.Dentin dysplasiadentin sialophosphoprotein genedentinogenesis imperfectaJournal ArticleIndiaDepartment of Oral and Maxillofacial Pathology and Oral Microbiology, ITS Centre for Dental Studies and Research, Ghaziabad, Uttar Pradesh, India