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Article

Dentin dysplasia, type II linkage to chromosome 4q.

Journal of craniofacial genetics and developmental biology - 1 Jan 2000

Dean J A, Hartsfield J K, Wright J T, Hart T C

Abstract excerpt

Dentin dysplasia, type II (MIM*125420) is an autosomal dominant disorder of dentin development. Clinically the primary dentition appears opalescent, and radiographically the pulp chambers are obliterated, resembling dentinogenesis imperfecta. However, unlike dentinogenesis imperfecta, the permanent teeth in dentin dysplasia, type II are normal in color and, on radiographs, have a thistle-tube pulp chamber...

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PMID: 9493074

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