Diseases [C] » Stomatognathic Diseases [C07] » Stomatognathic System Abnormalities » Tooth Abnormalities » Dentin Dysplasia
Diseases [C] » Stomatognathic Diseases [C07] » Tooth Diseases » Tooth Abnormalities » Dentin Dysplasia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Stomatognathic System Abnormalities » Tooth Abnormalities » Dentin Dysplasia
Description
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) MeSH
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