Abstract
Introduction: Crouzon syndrome is a genetic disease characterized by cranial and facial deformities, as well as several dental dysfunctions. Objectives: The main objective of the review is to analyze and highlight factors associated with oral, facial and dental development as consequences in the life of people with Crouzon Syndrome, highlighting its development, functional and aesthetic changes in addition to their respective treatments and results. Methodology: The LILACS, MEDLINE and SciELO databases were used as a methodology, and the terms “Crouzon syndrome”, “dental consequences”, “functional” and “aesthetic” were applied to the research. Results: Based on the research, it was found that the patients with the syndrome had several oral and facial manifestations that significantly interfered in their lives, requiring specific attention and care so that their clinical conditions did not worsen. Conclusion: Therefore, follow-up and surgical and orthodontic treatments, with multiprofessional performance, should be performed even in the infancy of these people in order to obtain better results and a good evolution.
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