Dental and Craniofacial Anomalies Associated with Axenfeld-Rieger Syndrome with PITX2 Mutation

Axenfeld-Rieger syndrome (ARS) (OMIM Nr.: 180500) is a rare autosomal dominant disorder (1  :  200000) with genetic and morphologic variability. Glaucoma is associated in 50% of the patients. Craniofacial and dental anomalies are frequently reported with ARS. The present study was designed as a mult...

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Detalles Bibliográficos
Autores principales: Dressler, Simone, Meyer-Marcotty, Philipp, Weisschuh, Nicole, Jablonski-Momeni, Anahita, Pieper, Klaus, Gramer, Gwendolyn, Gramer, Eugen
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2842968/
https://www.ncbi.nlm.nih.gov/pubmed/20339518
http://dx.doi.org/10.1155/2010/621984

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2842968/
https://www.ncbi.nlm.nih.gov/pubmed/20339518
http://dx.doi.org/10.1155/2010/621984

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