| Literature DB >> 15747651 |
Abstract
Amelogenesis imperfecta (AI) is an inherited enamel dysplasia involving both dentitions with no other systemic effects. The hereditary pattern is autosomal or X-related dominant or recessive. Its prevalence is approximately 1:14,000-1:16,000. It can be classified as hypocalcified, hypoplastic and hypomaturated according to clinical, radiological, histological and hereditary findings. This study presents a case of hypomaturated type AI in a 16-year-old young man that was successfully treated with different types of resin composites. The patient was regularly recalled during the one-year postoperative period. Radiographic and clinical examinations at recall revealed no evidence of complications associated with the restored teeth or their supporting structures.Entities:
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Year: 2005 PMID: 15747651 DOI: 10.1111/j.1875-595x.2005.tb00030.x
Source DB: PubMed Journal: Int Dent J ISSN: 0020-6539 Impact factor: 2.512