Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1993 Nov-Dec;15(6):384-93.

Clinical diagnosis and management strategies of amelogenesis imperfectavariants

Affiliations
  • PMID: 8152999

Clinical diagnosis and management strategies of amelogenesis imperfectavariants

W K Seow. Pediatr Dent. 1993 Nov-Dec.

Abstract

Amelogenesis imperfecta (AI) is a group of inherited disorders primarily affecting dental enamel. Variants of AI generally are classified as hypoplastic, hypocalcified, or hypomaturation types based on the primary enamel defect. The aim of this study was to analyze the clinical presentations, diagnostic features, and clinical complications of different variants of AI. Thirty-two patients from 17 families with several subtypes of AI were studied. The results showed that distinctive clinical features may be observed in each variant. However, all AI patients suffered common clinical problems of poor esthetics, teeth sensitivity, and loss of occlusal vertical dimension. The mildest problems were found in the pitted hypoplastic type whereas the most severe problems were encountered in the hypocalcified type of AI. Management strategies include composite resin veneers and jacket crowns for anterior teeth as well as steel crowns for posterior teeth. Knowledge of the clinical features and dental complications of each variant of AI helps in the diagnosis of the condition and allows institution of early preventive measures.

PubMed Disclaimer