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Dentin dysplasia: A genetic condition characterized by abnormal dentin in primary and/or secondary teeth. Dentin is the calcified structure directly under the outer tooth enamel but surrounding the inner tooth pulp. There are three subtypes of the condition with variable symptoms. More detailed information about the symptoms, causes, and treatments of Dentin dysplasia is available below.
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An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed) - (Source - Diseases Database)
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