TY - JOUR
T1 - Axenfeld-Rieger syndrome
T2 - a case report
AU - Dunbar, A. Craig
AU - McIntyre, Grant T.
AU - Laverick, Sean
AU - Stevenson, Brian
PY - 2015
Y1 - 2015
N2 - Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant condition manifesting as a heterogeneous group of features. Of particular note are the ocular and craniofacial anomalies and dental features such as hypodontia, microdontia, taurodontism, enamel hypoplasia, conical-shaped teeth, shortened roots and delayed eruption. To treat cases with ARS effectively, a multidisciplinary approach is required, and this report describes the complex and long-term management of a case with input from Paediatric Dentistry, Orthodontics, Restorative Dentistry, Speech and Language Therapy, Oral and Maxillofacial Surgery and Radiology.
AB - Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant condition manifesting as a heterogeneous group of features. Of particular note are the ocular and craniofacial anomalies and dental features such as hypodontia, microdontia, taurodontism, enamel hypoplasia, conical-shaped teeth, shortened roots and delayed eruption. To treat cases with ARS effectively, a multidisciplinary approach is required, and this report describes the complex and long-term management of a case with input from Paediatric Dentistry, Orthodontics, Restorative Dentistry, Speech and Language Therapy, Oral and Maxillofacial Surgery and Radiology.
U2 - 10.1179/1465313315Y.0000000017
DO - 10.1179/1465313315Y.0000000017
M3 - Article
C2 - 26281856
SN - 1465-3125
VL - 42
SP - 324
EP - 330
JO - Journal of Orthodontics
JF - Journal of Orthodontics
IS - 4
ER -