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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The anamnesis showed good general health, no history of dental or facial trauma and no previous orthodontic treatment. 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 dwntinaria condition.
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The patient referred a solid mass in the area described. International collaborative study on ghost cell odontogenic tumours: Overjet and overbite were moderate and both the upper and lower dental midlines were deviated to the right side Figs 8 and 9. Amelogenesis imperfecta Dentinogenesis imperfecta Dentin dysplasia Regional odontodysplasia. This article needs additional citations for verification. Dentin dysplasia is a rare defect of dentin development with an autosomal dominant pattern of inheritance, which is generally divided into 2 main classes based on the clinical and radiographic appearance of the affected dental tissues: Orphanet Journal of Rare Diseases.
Repair of root resorption 4 and 8 weeks after application of continuous light and heavy forces on premolars for 4 weeks: Discussion In the WHO classification defined specific types of cystic lesions and solid tumor mass as well as their development.
Orthodontic movement of teeth with short root anomaly: should it be avoided, faced or ignored?
The authors declare that procedures conformed to the ethical standards of the responsible committee on human experimentation and in accordance with the World Medical Association and the Declaration of Helsinki. Fronto-orbital sphenoidal fibrous dysplasia. The upper diplasia canine erupted in an infralabial inclined position, while the upper left canine was partially erupted due to space deficiency.
Tewari N, Pandey RK. Taurodontism in 47 XXY males: Arch Oral Biol ; The same procedure should be recommended in cases of movement in incisors with SRA, in order to contain excessive tooth mobility and ensure long-term stability.
Dental X-rays is the key to diagnose dentine dysplasia, especially on permanent teeth. Dental arch morphology and facial balance were also considered satisfactory at the end of the treatment Figs 19 and Neither pulp chamber obliteration nor periapical radiolucencies were observed in any of the panoramic radiographic images, which were confirmed by periapical radiograph Fig. Both primary and permanent dentitions can be affected by either type I or type II dentin dysplasia.
Behavior of short-rooted teeth in the upper bilateral central incisors.
Eur J Oral Sci. Van Dis and Allen 4 reported four cases of DD1 in which the radiographic features were somewhat different from those of other cases. Dentin dysplasia is a rare defect of dentin development with an autosomal dominant pattern of inheritance 1,2 that affects one in everyindividuals 3,4 and manifests in both primary 2, and permanent 2,5, dentitions.
Stainless steel crowns which also known as “hall crowns” can prevent tooth wear and maintain occlusal dimension in affected primary teeth. Seow WK, Shusterman S. Endodontic treatment is not advised for teeth with complete obliteration of root canals and pulp chambers.
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. Treatment of a patient with severely shortened maxillary central incisor roots. All of them had recurrences after surgical removal, diagnosed between first and eighth year of follow up.
In addition, recently, Sun G. It should be noted that there is no consensus regarding the best treatment option in cases of DGCT. The early solid variant of COC type II seemed to have a more aggressive development than cystic lesions; this could explain the common recurrent local sprouting after more traditional dipslasia protocols.
Clinical, radiographic, and histological manifestations of dentin dysplasia, type I: The facial examination showed a brachyfacial dfntinaria without any obvious skeletal asymmetry, convex facial profile, small nasal projection, and an acceptable nasolabial angle. A differential diagnosis of SRA should be conducted for teeth with incomplete root formation, external apical root resorption, dentin dysplasia type I and post dental trauma root hypoplasia.
Characteristics of permanent teeth in persons with trisomy G. Case report and treatment review. Cast partial dentures could also be an alternative treatment option and it only works if there are a few teeth that has enough root length to serve as retentive purpose.
Fibrous displasia: Report three cases
The intraoral clinical examination revealed the presence of the following teeth: O fibroma ossificante, apesar do crescimento lento, pode ter localmente comportamento mais agressivo.
Type I has been known as radicular dentine dysplasia dissplasia the teeth have undeveloped root s with abnormal pulp tissue.
J Nihon Univ Sch Dent. Localized deficient root development associated with taurodontism: Disturbances in the oral cavity in pediatric long-term survivors after different forms of antineoplastic therapy. Morphological characteristics of dentitions developing excessive root resorption during orthodontic treatment. However, no evidence of pulp chamber obliteration or periapical radiolucencies was found.
The affected root is smaller or presents the same size of the dental crown, has a tendency towards bilateral involvement and presents no other etiological factors.