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Published in: BMC Oral Health 1/2018

Open Access 01-12-2018 | Case report

Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports

Authors: Steve Toupenay, Benjamin Philippe Fournier, Marie-Cécile Manière, Chantal Ifi-Naulin, Ariane Berdal, Muriel de La Dure– Molla

Published in: BMC Oral Health | Issue 1/2018

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Abstract

Background

Hereditary enamel defect diseases are regrouped under the name “Amelogenesis Imperfecta” (AIH). Both dentitions are affected. Clinical expression is heterogeneous and varies between patients. Mutations responsible for this multigene disease may alter various genes and the inheritance can be either autosomal dominant or recessive, or X-linked. Until now, no therapeutic consensus has emerged for this rare disease.

Case presentation

The purpose of this article was to report treatments of AIH patients from childhood to early adulthood. Treatment of three patients of 3, 8 16 years old are described. Each therapeutic option was discussed according to patients’ age and type of enamel alteration. Paediatric crowns and resin based bonding must be preferred in primary teeth. In permanent teeth, non-invasive or minimally invasive dentistry should be the first choice in order to follow a therapeutic gradient from the less invasive options to prosthodontic treatments.

Conclusion

Functional and aesthetic issues require patients to be treated; this clinical care should be provided as early as possible to enable a harmonious growth of the maxillofacial complex and to prevent pain.
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Metadata
Title
Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports
Authors
Steve Toupenay
Benjamin Philippe Fournier
Marie-Cécile Manière
Chantal Ifi-Naulin
Ariane Berdal
Muriel de La Dure– Molla
Publication date
01-12-2018
Publisher
BioMed Central
Published in
BMC Oral Health / Issue 1/2018
Electronic ISSN: 1472-6831
DOI
https://doi.org/10.1186/s12903-018-0554-y

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