Dentin dysplasia type 1d: A rare case.
Article
Dans Anglais
| IMSEAR
| ID: sea-156567
ABSTRACT
Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by a 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 by pulp stones, short, blunted and malformed or absent roots, peri‑apical radiolucencies of noncarious teeth. We present a case of dentin dysplasia type 1d in a 19‑year‑old boy along with the clinical, radiographic findings of this condition and treatment. There 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.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Humains
/
Mâle
/
Adolescent
/
Pulpe dentaire
/
Dysplasie de la dentine
langue:
Anglais
Année:
2014
Type:
Article
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