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Syndromes/Craniofacial Anomalies

357 - Amelogenesis Imperfecta: A Case Report

Friday, May 24, 2024
4:15 PM – 4:25 PM EST
Location: Exhibit Hall (back left corner of the hall, space 137)

    Presenting Author(s)

  • Mollie Mahoney, DDS

    Pediatric Dental Resident
    University of Michigan
    University of Michigan
    Ann Arbor, Michigan, United States

    • Program Director(s)

  • JB

    James R. Boynton, DDS, MS

    Clinical Professor and Program Director
    University of Michigan
    Ann Arbor, MI, Michigan, United States

Abstract: Amelogenesis imperfecta is a group of rare genetic disorders that affects the enamel formation in both primary and permanent teeth. There are three major categories of amelogenesis imperfecta: hypoplastic, hypocalcified, and hypomaturation. This case report details the evaluation and treatment options of a 13 year 11 month old male with hypoplastic amelogenesis imperfecta.

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