Oral Phenotype of Singleton–Merten Syndrome: A Systematic Review Illustrated With a Case Report

Background: Singleton–Merten syndrome type 1 (SGMRT1) is a rare autosomal dominant disorder caused by IFIH1 variations with blood vessel calcifications, teeth anomalies, and bone defects. Aim: We aimed to summarize the oral findings in SGMRT1 through a systematic review of the literature and to desc...

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Detalles Bibliográficos
Autores principales: Riou, Margot Charlotte, de La Dure-Molla, Muriel, Kerner, Stéphane, Rondeau, Sophie, Legendre, Adrien, Cormier-Daire, Valerie, Fournier, Benjamin P. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218817/
https://www.ncbi.nlm.nih.gov/pubmed/35754802
http://dx.doi.org/10.3389/fgene.2022.875490

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218817/
https://www.ncbi.nlm.nih.gov/pubmed/35754802
http://dx.doi.org/10.3389/fgene.2022.875490

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