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Dentin Dysplasia, Coronal
Condition Overview: Coronal dentin dysplasia is a rare inherited dental defect that is also known as dentin dysplasia, type II. It is characterized by abnormal development (dysplasia) of the hard tissue (i.e., dentin) that is beneath the enamel, surrounds the pulp, and forms the major part of the teeth. In those with coronal dentin dysplasia, the baby teeth (primary or deciduous teeth) are brownish blue with a translucent "opalescence." (Opalescence refers to a milky, opal-like display of colors in reflected light [iridescence].) However, the permanent teeth appear normal in color.As seen on dental x-ray imaging, the pulp chambers of the primary teeth--or the natural cavities that contain living pulp in the exposed portion of the teeth (crowns)--are obliterated by abnormal dentin. In addition, the pulp-containing canals within the roots of the teeth (root canals) are smaller than normal. The permanent teeth also have distinctive abnormalities of the pulp chambers. Coronal dentin dysplasia is transmitted as an autosomal dominant trait. . |
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