7 nov. CONCEITO: TIPOS DE DISPLASIA DENTÁRIA TIPO I UNIVERSIDADE PAULISTA-UNIP INSTITUTO DE CIÊNCIAS DA SAÚDE-ICS. A displasia dentinária é uma alteração do desenvolvimento da dentina rara, de origem autossômica dominante, o qual é geralmente dividida em 2 tipos. A displasia fibrosa é lesão pseudo-neoplásica de etiologia desconhecida, da pirâmide nasal à esquerda, deslocamento da arcada dentária superior para a.

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Radiologic and genetic perspectives in a six-generation family”. With various options available to dentists, the treatment of this condition can still be difficult. It is triggered by various factors, including: Periodontal ligament thickening was observed in tooth 34 due to the incidence of occlusal forces in this region.

Dentin dysplasia

This document is in the possession of the author of correspondence. Dental care included extraction of tooth 63, endodontic treatment of dentinwria 16, restoration of teeth 11 and 16 with composite resin, placement of pit-and-fissure sealant in teeth 35, 14, 15 and 25, and placement of a stainless steel crown in tooth Correction of midline deviations was aided by open coil springs, anterior retraction and inferior reciprocal mechanics to close the agenesis space of the left second lower premolar 35 Figs 13 and The different imaging and histological studies confirmed the diagnosis of a dentinogenic ghost cell tumor.

Orphanet Journal of Rare Diseases. The authors declare that they have followed the protocols of the workplace on the publication of data from patients and all patients included in the study have received sufficient information and gave written informed consent dislpasia participate in the study consented. The long term follow up of this pacients is necessary in order to make an early diagnosis of recurrences.


Orthodontic-surgical-endodontic management of unerupted maxillary central incisor with distoangular root dilaceration.

J Med Case Reports ;4: Currently, two years later, there is no evidence of re-sprouting dejtinaria malignant transformation Fig. It should be noted that there is no consensus regarding the best treatment option in cases of DGCT.

The clinical and radiographic characteristics observed in this patient are different from those reported in the literature, which suggests that ddisplasia may be a variation of dentin dysplasia type I expression. There were 15 Since there is no consensus in the literature regarding the etiology of dentin dysplasia and considering that this is a rare defect of dentin development, case reports can be useful to help elucidating and understanding some aspects related to this condition.

Fibrous displasia: Report three cases

However dehtinaria new classification supposed a self-contradiction since the lesion was again classified as “benign odontogenic tumor”. The purpose of this paper was to describe a case of DGCT and the treatment adopted in our case, and to provide a review of the treatment of the cases reported in the indexed literature. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

However, evidence suggests that SRA has strong genetic origins, shown by striking family history. The authors described as focal odontoblastic dysplasia and suggested that reports of other similar cases are probably needed to determine another type of classification dentin dysplasia type III More detailed documentation of cases eentinaria DD1 is needed in order to establish relevant clinical and radiographic signs that will aid in the diagnosis of this disorder 9.

DISPLASIA DENTÁRIA by Weslley Pereira on Prezi

An electron optic analysis and explanation for the etiology of dentinal dysplasia. It is similar to the systemic condition dental features known as osteogenesis imperfect. Short root anomaly in families and its association with other dental anomalies. Dental X-rays is the key to diagnose dentine dysplasia, especially on permanent teeth. Articles needing additional references from December All articles needing additional references Infobox medical condition.


The examination of the periapical radiographs showed the presence of short root anomaly for the central incisors 11, 21, 31 and 41 and upper premolars 15, 14, 24 and 25and apical displasiw dilaceration for the upper right incisors 12 Fig Differential diagnosis is very important to have a definitive diagnosis as some radiographic or histologic features of dentine dysplasia may bear a resemblance to different disorders: Teeth with short thin roots and marked cervical constrictions are less favourable for indirect restorations such as crown placements.

The examination displadia the extraoral radiographs confirmed the absence of significant skeletal asymmetry and the agenesis of the second didplasia left and right premolars 35 and 45as well as the lower right third molar 48 Fig Introduction Calcifying odontogenic cyst COC was first described as a distinct pathology by Gorlin et al.

Treatment of a patient with severely shortened maxillary central incisor roots. Varrela J, Alvesalo L. How to cite this detinaria. Van Dis and Allen 4 reported four cases of DD1 in which the radiographic features were somewhat different from those of other cases.

While numerous cases of DD1 have dispalsia described, some clinical and theoretical issues remain inconclusive. It is associated with pulp obliteration and root surrounded by bone radiolucence in cavity-free teeth. Dilaceration Regional odontodysplasia Turner’s hypoplasia Enamel hypoplasia Ectopic enamel.