Dentin dysplasia type 1 - clinical management dilemmas: A case report of first-generation sufferers.

J Indian Soc Pedod Prev Dent

Department of Pedodontics and Preventive Dentistry, GDC, Amritsar, Punjab, India.

Published: October 2018

Dentine Dysplasia is a rare genetic condition. The treatment options and dilemmas associated with the condition remain undiscovered so far. This article highlights the variations in traits and challenges faced in the treatment of the cases.

Download full-text PDF

Source
http://dx.doi.org/10.4103/JISPPD.JISPPD_1127_17DOI Listing

Publication Analysis

Top Keywords

dentin dysplasia
4
dysplasia type
4
type clinical
4
clinical management
4
management dilemmas
4
dilemmas case
4
case report
4
report first-generation
4
first-generation sufferers
4
sufferers dentine
4

Similar Publications

Segmental Odontomaxillary Dysplasia: Unusual Tumoral Lesion.

Head Neck Pathol

January 2025

Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Introduction: Segmental Odontomaxillary Dysplasia (SOD) is a non-hereditary, unilateral developmental anomaly recently included in the WHO's classification of head and neck tumors.

Case Presentation: Here, we report the case of an 8-year-old boy presenting with unilateral maxillary enlargement and pain without facial asymmetry. Computed tomography revealed a hypodense area in the maxillary bone with altered bone structure and osseous expansion.

View Article and Find Full Text PDF

The purpose of this article is to present three cases of a rare phenomenon called pre-eruptive coronal resorption (PCR), which occurs in teeth with enamel degeneration. In the first case, the enamel defects occurred due to ectodermal dysplasia, which represents the first documented case of a patient with ectodermal dysplasia who underwent PCR. In the other two cases, the enamel defects occurred due to amelogenesis imperfecta.

View Article and Find Full Text PDF

The sulfate transporter gene SLC26A2 is crucial for skeletal formation, as evidenced by its role in diastrophic dysplasia, a type of skeletal dysplasia in humans. Although SLC26A2-related chondrodysplasia also affects craniofacial and tooth development, its specific role in these processes remains unclear. In this study, we explored the pivotal roles of SLC26A2-mediated sulfate metabolism during tooth development.

View Article and Find Full Text PDF
Article Synopsis
  • This study investigates the effects of excessive fluoride on the microstructure of dentine in mice, as previous research has mostly focused on its impact on enamel.* -
  • Male C57BL6/J mice were divided into four groups, receiving different fluoride concentrations in their drinking water for six weeks, after which various analyses were conducted to evaluate enamel and dentine properties.* -
  • Results indicated that high fluoride exposure (50-125 ppm) led to enamel hypoplasia, reduced dentine mineral density, and changes in the structure of the dentine-pulp complex, demonstrating significant negative effects of excessive fluoride consumption.*
View Article and Find Full Text PDF

Dentin dysplasia (DD) is a rare clinical entity that can affect deciduous dentition alone, or both deciduous and permanent dentition. It is a developmental disorder that can be classified as DD type I or type II. This case report describes a rare case of DD type I in a 19-year-old patient, highlighting the clinical presentation and the radiographic features of the condition, confirmed by ground sectioning and microscopic examination of extracted teeth.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!