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Related Experiment Videos

Dentinogenesis imperfecta type III with enamel and cementum defects.

S Clergeau-Guerithault, J R Jasmin

    Oral Surgery, Oral Medicine, and Oral Pathology
    |May 1, 1985
    PubMed
    Summary

    This study examined primary teeth with no enamel and large pulp chambers, suggesting a rare condition called odontodysplasia. This rare dental anomaly was found in a case of dentinogenesis imperfecta type III.

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    Annales de pediatrie·1993

    Area of Science:

    • Pediatric Dentistry
    • Dental Morphology
    • Developmental Biology

    Background:

    • Primary teeth anomalies require careful diagnosis.
    • Dentinogenesis imperfecta type III is a rare inherited disorder affecting dentin formation.
    • Odontodysplasia presents with developmental defects in enamel and dentin.

    Observation:

    • Examination of ground sections and scanning electron microscopy (SEM) of primary teeth.
    • The teeth belonged to a 2-year-old child.
    • Observed features included complete absence of enamel and unusually large pulp chambers.

    Findings:

    • The observed dental anomalies suggest a diagnosis of odontodysplasia.
    • The case was classified within the spectrum of dentinogenesis imperfecta type III.
    • Combined features indicate a complex developmental defect affecting tooth structure.

    Implications:

    • Highlights the importance of detailed microscopic analysis in diagnosing rare dental conditions.
    • Contributes to understanding the phenotypic variability of dentinogenesis imperfecta.
    • Informs clinical management strategies for children with severe tooth structure abnormalities.

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