Nonsyandromic oligodontia: A rare case report

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Abstract

Dental agenesis is the most common developmental anomaly in humans, which can be either in the form of anodontia, oligodontia, or hypodontia. Oligodontia can occur either as an isolated finding or as part of a syndrome. Nonsyndromic oligodontia is rare. Management requires integrated multidisciplinary approach. Prompt intervention improves quality of life. Here, we report a case of isolated, nonsyndromic oligodontia in a 13-year-old female who allegedly had complete set of primary teeth but failed to develop complete permanent dentition. No other clinical feature, except oligodontia, was present that could suggest any syndromic association.

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Chaturvedi, M., Thakkar, J., Thaddanee, R., & Khilnani, A. (2015). Nonsyandromic oligodontia: A rare case report. Medical Journal of Dr. D.Y. Patil University, 8(3), 337–339. https://doi.org/10.4103/0975-2870.157079

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