Dentin Dysplasia Type I: A Rare Case Report and Management Protocol

Shimasadat Miri¹, Mahsasadat Miri², Parisa Soltani^3, and Amirhossein Moaddabi⁴

¹Department of Endodontics, School of Dentistry, Kermanshah University of Medical Sciences, Kermanshah, Iran

²Department of Obstetrics and Gynecology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

³Department of Oral and Maxillofacial Radiology, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran

⁴Department of Oral and Maxillofacial Surgery, School of Dentistry, Mazandaran University of Medical Sciences, Sari, Iran

Cite this paper:
Shimasadat Miri, Mahsasadat Miri, Parisa Soltani and Amirhossein Moaddabi. Dentin Dysplasia Type I: A Rare Case Report and Management Protocol. International Journal of Dental Sciences and Research. 2017; 5(5):122-124. doi: 10.12691/ijdsr-5-5-2

Abstract

Dentin Dysplasia (DD) is a rare autosomal dominant anomaly that disturbs the formation of dentin in primary and/or permanent dentitions. This condition is classified into types I (radicular) and II (coronal) based on radiological findings. A case of DD type I in an 11-year old Iranian boy is presented and the clinical and radiological findings and selected treatment plan are discussed.

Keywords:
dentin dysplasia radicular pediatric dentistry

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