Ciola B, Bahn S L, Goviea G L
Oral Surg Oral Med Oral Pathol. 1978 Feb;45(2):317-22. doi: 10.1016/0030-4220(78)90101-9.
Dentin dyslasia is a rare autosomal dominant hereditary variant of dentinogenesis imperfecta. The primary defect is mesodermal and involves the dentin. Two types (Type I and Type II) of dentin dysplasia have been described previously. The current case presents radiographic findings which include characteristics common to both types. It is proposed that either a third type (Type III) be recognized or the variability of the developmental defect precludes definitive subclassification.
