Open AccessClinical management of Hypoplasic Amelogenesis Imperfecta: a challenge for multidisciplinary team. A case report
Author(s) -
María Gabriela Acosta-de Camargo,
Alfredo Enrique Natera-Guarapo,
John Mangles
Publication year - 2021
Publication title -
revista facultad de odontología universidad de antioquia/revista de la facultad de odontologia universidad de antioquia
Language(s) - English
Resource type - Journals
eISSN - 2145-7670
pISSN - 0121-246X
DOI - 10.17533/udea.rfo.v33n1a10
Subject(s) - amelogenesis imperfecta , medicine , odontogenic , multidisciplinary approach , physical examination , dentistry , intervention (counseling) , orthodontics , occlusion , clinical diagnosis , enamel paint , intensive care medicine , surgery , pathology , psychiatry , social science , sociology
Amelogenesis imperfecta (AI) refers to a group of rare genetic disorders that involve tooth development and are passed down through families. Hypoplasic AI phenotypes include the absence of enamel as a result of a defect in the secretory stage. This case report describes the diagnosis and treatment of a patient with hypoplastic AI. The clinical implications include sensitive teeth, functional problems, and aesthetic complaining. The diagnosis was done through history, clinical examination and imaging. The intervention was performed by Direct Resin Veneers. This treatment showed to improve occlusion, esthetics, and selfimage of the teenager. The satisfactory clinical result has made it possible to avoid more invasive and expensive treatments.