Open AccessAmelogenesis imperfecta: A case series
Author(s) -
M J Jijin,
P P Thabsheera,
Mohamed Labeeb K P,
R Anjana
Publication year - 2021
Publication title -
ip international journal of maxillofacial imaging/international journal of maxillofacial imaging/ip international journal of maxillofacial imaging
Language(s) - English
Resource type - Journals
eISSN - 2581-382X
pISSN - 2455-6750
DOI - 10.18231/j.ijmi.2021.026
Subject(s) - amelogenesis imperfecta , permanent dentition , dentition , enamel paint , dentistry , orthodontics , medicine , amelogenesis , dental enamel , psychology
Amelogenesis imperfecta (AI) refers to a group of rare genetic disorders that involve tooth development and that are passed down through families as a dominant trait. This condition is characterized by abnormal enamel formation caused by gene mutations that alter the quality and/or quantity of enamel. This dental problem can impact both primary and permanent dentition, varies among affected individuals, and results in esthetic and functional problems. The treatment planning for patients with AI is related to many factors, including the age of the patient, the type and severity of the disorder, intraoral conditions, and the socioeconomic status of the patient. It is crucial to plan a proper remedy, which requires collaboration among dental specialties to execute comprehensive dental treatment in order to provide a long-term solution with adequate esthetics. This clinical case study looks at three different types of amelogenesis imperfecta patients.