A histological continuum between dentinogenesis imperfecta and dentin dysplasia: A case report with literature review
نویسندگان
چکیده
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...
متن کاملDentin 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 ...
متن کاملCASE 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...
متن کاملDentin dysplasia type I: a case report and review of the literature
INTRODUCTION Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious ...
متن کاملOsteogenesis Imperfecta: A Case Report and Review of Literature
Osteogenesis imperfecta (OI) is a group of rare inherited disorders of connective tissue with the common feature of excessive fragility of bones caused by mutations in collagen. Diagnosis is mainly based on the clinical features of the disorder. We report, the case of a male neonate delivered to a 33-year-old para 2 female at University of Nigeria Teaching Hospital, Enugu with no family history...
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ژورنال
عنوان ژورنال: Indian Journal of Dental Research
سال: 2019
ISSN: 0970-9290
DOI: 10.4103/ijdr.ijdr_318_18