Dentin Dysplasia: ARare Case Report
نویسندگان
چکیده مقاله:
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 root defects in the periapical radiography, is introduced. Conclusion:Regarding the root defect only in the anterior mandibular teeth, it seems to be a regional dentin dysplasia.
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 کاملCASE 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...
متن کاملDentin 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...
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 کاملSolitary plasmacytoma of the thumb: Arare case report
A solitary plasmacytoma of bone occurs in approximately 2-5% of patients with myeloma. The lesion mostly found in the axial skeleton and have infrequently been reported to arise in the hand, and usually occur in the distal phalanges. We report the interesting case of a 75-year-old man who developed a solitary lytic lesion of the thumb proximal phalanx. This lesion was explored through MR imagin...
متن کاملBone Fibrosis Dysplasia - Gastrointestinal Case Report
Un cas de fihreuse dysplasie evoluant dcpuis dix ans a ete observe a l'hopital farahnaz de l'universite Melli de Teheran. La particu-larite in terssante de cettc patiente est tout d'abord la clegenerscence kystiquc de foyer de l'os iliaque droit et la multitude des fractures des membres ayant consolide dans des positions v1cieusc spon tanement. Presence d'un foyer temporal gauchf! de .forme scl...
متن کاملمنابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ذخیره در منابع من قبلا به منابع من ذحیره شده{@ msg_add @}
عنوان ژورنال
دوره 14 شماره 2
صفحات 71- 78
تاریخ انتشار 2019-07
با دنبال کردن یک ژورنال هنگامی که شماره جدید این ژورنال منتشر می شود به شما از طریق ایمیل اطلاع داده می شود.
کلمات کلیدی برای این مقاله ارائه نشده است
میزبانی شده توسط پلتفرم ابری doprax.com
copyright © 2015-2023