Enamel and dentin in Enamel renal syndrome: A confocal Raman microscopy view

Enamel and dentin in Enamel renal syndrome: A confocal Raman microscopy view

Enamel Renal Syndrome (ERS) is a rare genetic disorder caused by biallelic mutations in Family with sequence similarity 20A (FAM20A) gene encoding the secretory pathway pseudokinase FAM20A. ERS is characterized by hypoplastic amelogenesis imperfecta (AI), impaired tooth eruption, intra-pulpal calcif...

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Bibliographic Details
Main Authors: Alban Desoutter, Olivier Cases, Pierre Yves Collart Dutilleul, Victor Simancas Escorcia, Vidjea Cannaya, Frédéric Cuisinier, Renata Kozyraki
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Physiology
Subjects:
confocal Raman microscopy
enamel
dentin
dentin enamel junction
enamel renal syndrome
amelogenesis imperfecta
Online Access:https://www.frontiersin.org/articles/10.3389/fphys.2022.957110/full

Internet

https://www.frontiersin.org/articles/10.3389/fphys.2022.957110/full

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