Dentinal dysplasia

Logan, James G.; Becks, Hermann; Silverman, S; Pindborg, J. J.

doi:10.1016/0030-4220(62)90113-5

Cited by 49 publications

(21 citation statements)

References 2 publications

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“…Logan et al . [7] proposed that it is the dentinal papilla that is responsible for the abnormalities in root development. They suggested that multiple degenerative foci within the papilla become calcified, leading to reduced growth and final obliteration of the pulp space.…”

Section: Discussionmentioning

confidence: 99%

Dentin dysplasia type I: a case report and review of the literature

et al. 2010

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IntroductionDentin 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 teeth.Case presentationWe present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described.ConclusionsThere are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition.

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Section: Discussionmentioning

confidence: 99%

Dentin dysplasia type I: a case report and review of the literature

et al. 2010

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“…In some ways, it could be related to dentinal dysplasia, as it was first described by Logan et al 19 In both cases, normal cusps and a normal mantle dentin layer are found, whereas the rest of the dentin is severely disturbed, and the roots are shortened. However, in dentinal dysplasia, all teeth (not only quadrants) are affected.…”

Section: Resultsmentioning

confidence: 89%

Structural, Ultrastructural, Microradiographic, and Electron-probe Studies of an Unusual Case of Regional Odontodysplasia

Kerébel

Kerebel

1982

J Dent Res

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“…Logan et al 9 proposed that it is the dentinal papilla that is responsible for the abnormalities in root development. They suggested that multiple degenerative foci within the papilla become calcified, leading to reduced growth and final obliteration of the pulp space.…”

Section: Discussionmentioning

confidence: 99%

Dentin dysplasia type I

et al. 2013

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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 dentitions. Radiographic analysis shows obliteration of all pulp chambers, short, blunted, and malformed roots, and periapical radiolucencies of non-carious teeth. This paper presents three cases demonstrating classic features of type I dentin dysplasia.

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Dentinal dysplasia

Cited by 49 publications

References 2 publications

Dentin dysplasia type I: a case report and review of the literature

Dentin dysplasia type I: a case report and review of the literature

Structural, Ultrastructural, Microradiographic, and Electron-probe Studies of an Unusual Case of Regional Odontodysplasia

Dentin dysplasia type I

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