Management of dentin dysplasia and facial disharmony

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چکیده

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Management of dentin dysplasia and facial disharmony.

D ENTIN DYSPLASIA was first reported in 1922 by Ballschmiedel who described six children in one family whose teeth had short, blunted roots with pulpal occlusion that he called “rootless teeth.” Rushton2 later described a similar condition in an individual without evidence of genetic inheritance that he labeled “dental dysplasia. ” Cases have been reported in the literature that describe dentin...

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Dentin Dysplasia: ARare Case Report

Introduction: Dentin Dysplasia is one of the rare hereditary diseases that the enamel is normal, but it also affects the dentin and  the shape of the tooth pulp. Due to the low prevalence of this disease, a case of dentin dysplasia with the classical and atypical dentin dysplasia type 1 is presented. Case presentation:A 11-year-old girl with the mobility of lower central teeth that has severe ...

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Developmental Disturbance of Dentin with Probable Diagnosis of Dentin Dysplasia Type 1d: A rare case report

Background: Dentin dysplasia (DD) is a rare disturbance of dentin formation, characterized by normal enamel but atypical dentin formation with abnormal pulpal morphology. In DD type I, the teeth appear clinically normal in morphologic appearance and color. Radiographic analysis shows obliteration of all pulp chambers as well as short, blunted, and malformed or absent roots with multiple periapi...

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CASE REPORT Dentin dysplasia type I

To cite: Singh A, Gupta S, Yuwanati MB, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013009403 SUMMARY Dentin dysplasia type I is a rare hereditary disturbance of dentin formation characterised clinically by nearly normal appearing crowns and hypermobility of teeth that affects one in every 100 000 individuals and manifests in both primary and permanent...

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ژورنال

عنوان ژورنال: Special Care in Dentistry

سال: 1983

ISSN: 0275-1879,1754-4505

DOI: 10.1111/j.1754-4505.1983.tb01615.x