4
Authors
10
References
2016
Year Published
Abstract
Dentinogenesis imperfecta (DI) is a developmental tooth disorder affecting dentin, characterized by the presence of opalescent dentin caused due to autosomal dominant pattern resulting in a greyish blue to brownish discoloration of the teeth. It can affect both deciduous as well as a permanent dentition. This case report describes a 26-year-old male patient with clinical and radiographical characteristic features of dentinogenesis imperfecta.
Keywords: Autosomal dominant, dentinogenesis imperfecta, dystrophic dentin, pulpal space obliteration.
How to Cite
Reddy J, Maybel C, Archana PS, Sivansatish. Dentinogenesis Imperfecta: Case Report and Review of Literature. J Indian Dent Assoc Madras. 2016;3(2):15-16. DOI: 10.37841/jidam_2016_V3_I2_03
Reddy, J., Maybel, C., Archana, P. S., & Sivansatish. (2016). Dentinogenesis Imperfecta: Case Report and Review of Literature. Journal of Indian Dental Association Madras, 3(2), 15-16. https://doi.org/10.37841/jidam_2016_V3_I2_03
Reddy, Jaget, et al. "Dentinogenesis Imperfecta: Case Report and Review of Literature." Journal of Indian Dental Association Madras, vol. 3, no. 2, 2016, pp. 15-16. DOI: 10.37841/jidam_2016_V3_I2_03.
Reddy J, Maybel C, Archana PS, Sivansatish. Dentinogenesis Imperfecta: Case Report and Review of Literature. J Indian Dent Assoc Madras. 2016;3(2):15-16. doi:10.37841/jidam_2016_V3_I2_03
Reddy, Jaget, Christeffi Maybel, P. Sai Archana, and Sivansatish. "Dentinogenesis Imperfecta: Case Report and Review of Literature." Journal of Indian Dental Association Madras 3, no. 2 (2016): 15-16. https://doi.org/10.37841/jidam_2016_V3_I2_03.
References
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