Dentin Dysplasia: ARare Case Report

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چکیده

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منابع مشابه

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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Dentin dysplasia type I--a case report.

A case report on dentin dysplasia type I, a congenital disease (autosomal dominant gene defect) affecting deciduous and permanent teeth, is depicted including representations of clinical and histological features, X-ray and CT-findings. Therapy includes extraction of all teeth, ectomization of cystic alteration, revision of paranasal sinus. Aesthetic and functional rehabilitation by means of in...

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CASE REPORT Spectrum of dentin dysplasia in a family: case report and literature review

The dentin dysplasias (DD), which may be classified as type I (DD1) or type 2 (DD2), form a group of rare, inherited abnormalities that are clinically distinct from dentinogenesis imperfecta. Studies of affected families may help to distinguish different types of DD and provide further insight into their etiology and clinical management. This report describes a family that showed characteristic...

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ژورنال

عنوان ژورنال: Iranian Journal of Pediatric Dentistry

سال: 2019

ISSN: 1735-8434,1735-8434

DOI: 10.29252/ijpd.14.2.71