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Title: [Hereditary type enamel hypoplasia. Clinical and histopathological findings of an observed case]. Author: Debernardi C, Pirrello D. Journal: Minerva Stomatol; 1989 Mar; 38(3):321-34. PubMed ID: 2657367. Abstract: The main classifications published in recent years on amelogenesis imperfecta are reported and the ways in which abnormal enamel can be formed are described. A personal case is reported in which it was possible to draw up a family tree and document clinical and histological histories. The anomaly was classified in the hypoplasia group, rough, autosomic dominant according Witkop and Sauk.[Abstract] [Full Text] [Related] [New Search]