Axenfeld–Rieger syndrome: orthopedic and orthodontic management in a pediatric patient: a case report

Axenfeld–Rieger Syndrome (ARS) is a rare autosomal dominant genetic disease with considerable expressive variability, characterized by ocular and non-ocular manifestations, cardiovascular, mild craniofacial abnormalities and dental malformations. Current data report an incidence of Xenfeld-Rieger sy...

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Detalles Bibliográficos
Autores principales: Cazzolla, Angela Pia, Testa, Nunzio Francesco, Spirito, Francesca, Di Cosola, Michele, Campobasso, Alessandra, Crincoli, Vito, Ballini, Andrea, Cantore, Stefania, Ciavarella, Domenico, Lo Muzio, Lorenzo, Dioguardi, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264492/
https://www.ncbi.nlm.nih.gov/pubmed/35804381
http://dx.doi.org/10.1186/s13005-022-00329-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264492/
https://www.ncbi.nlm.nih.gov/pubmed/35804381
http://dx.doi.org/10.1186/s13005-022-00329-y

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