Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations

De La Dure-Molla, M, Quentric, M, Yamaguti, PM et al. (6 more authors) (2014) Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations. Orphanet Journal of Rare Diseases, 9 (1). 84. ISSN 1750-1172



  • De La Dure-Molla, M
  • Quentric, M
  • Yamaguti, PM
  • Acevedo, A-C
  • Mighell, AJ
  • Vikkula, M
  • Huckert, M
  • Berdal, A
  • Bloch-Zupan, A
Copyright, Publisher and Additional Information: © 2014 de la Dure-Molla et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.
Keywords: Enamel Renal Syndrome (ERS); Amelogenesis Imperfecta and Gingival Fibromatosis syndrome (AIFGS); Enamel Dysplasia with Hamartomatous atypical Follicular Hyperplasia Syndrome (EDHFH); Amelogenesis Imperfecta; Enamel defect; Delayed tooth eruption; Intra-pulpal calcification; Gingival hyperplasia; FAM20A
  • Published: 14 June 2014
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Dentistry (Leeds) > Oral Surgery (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 23 Oct 2014 09:49
Last Modified: 07 Dec 2022 15:14
Published Version:
Status: Published
Publisher: BioMed Central
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