Bomfim, G.H.S., Dupont, G., Wright, T. et al. (2 more authors) (2025) Burden of hereditary enamel disorders. Trends in Molecular Medicine. ISSN: 1471-4914 (In Press)
Abstract
Dental enamel protects against the invasion of bacterial pathogens deep into the innervated layers of the tooth. Hereditary enamel disorders referred to as amelogenesis imperfecta (AI) can severely affect the development and mineralization of dental enamel compromising these functions. This rare disorder is often visible, carries a significant psychological and financial burden, and cosegregates with disease in other organs. Pathological variants in over 100 genes affect the enamel formation. Here, we describe the biology of enamel formation focusing on pathogenic variants underlying AI. We provide a computational model encapsulating new advances in calcium regulation during enamel formation. We also describe the psychological and financial burden of AI, its impact in systemic health, and discuss recent developments in diagnostic panels to detect AI.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | This is an author produced version of an article published in Trends in Molecular Medicine, made available under the terms of the Creative Commons Attribution License (CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. |
Keywords: | enamel, hereditary disease, gene variants, modeling calcium transport |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Dentistry (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 23 Jul 2025 13:15 |
Last Modified: | 23 Jul 2025 13:15 |
Published Version: | https://www.sciencedirect.com/science/article/pii/... |
Status: | In Press |
Publisher: | Elsevier |
Identification Number: | 10.1016/j.molmed.2025.06.002 |
Related URLs: | |
Sustainable Development Goals: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:229399 |
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