Article
A UK-based consensus on clinical decision flowcharts for managing childhood amelogenesis imperfecta in the permanent dentition.
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry - 1 Feb 2026
Lakhani S, Monteiro J, Agel M, Lyne A, Somani C, Balmer R, Mighell A, O'Donnell K, Lafferty F, McCann C, Parekh S
Abstract excerpt
PURPOSE: Amelogenesis imperfecta (AI) is a rare genetic condition characterised by defective enamel formation, with variable presentations. Diagnosis traditionally involves family history, clinical presentation, with genetic testing being increasingly integrated into clinical practice. Children and young people (CYP) with AI face clinical and psychosocial challenges over extended periods. Given the absence of...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
