Enamel Renal Syndrome: A Systematic Review

The enamel renal syndrome (ERS) is a rare autosomal recessive disease that is associated with mutations in the FAM20A gene. The syndrome is characterized by impaired amelogenesis of the hypoplastic type and nephrocalcinosis, presenting with presence of thin or absence of enamel, late dental eruption...

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Detalles Bibliográficos
Autores principales: Farias, Maria Luiza Morais, Ornela, Gabriela Oliveira, de Andrade, Rodrigo Soares, Martelli, Daniella Reis B., Dias, Verônica Oliveira, Júnior, Hercílio Martelli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101666/
https://www.ncbi.nlm.nih.gov/pubmed/33994680
http://dx.doi.org/10.4103/ijn.IJN_27_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101666/
https://www.ncbi.nlm.nih.gov/pubmed/33994680
http://dx.doi.org/10.4103/ijn.IJN_27_19

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