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Axenfeld-Rieger syndrome: a case report.
J Orthod. 2015; 42(4):324-30.JO

Abstract

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.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

26281856

Citation

Dunbar, A Craig, et al. "Axenfeld-Rieger Syndrome: a Case Report." Journal of Orthodontics, vol. 42, no. 4, 2015, pp. 324-30.
Dunbar AC, McIntyre GT, Laverick S, et al. Axenfeld-Rieger syndrome: a case report. J Orthod. 2015;42(4):324-30.
Dunbar, A. C., McIntyre, G. T., Laverick, S., & Stevenson, B. (2015). Axenfeld-Rieger syndrome: a case report. Journal of Orthodontics, 42(4), 324-30. https://doi.org/10.1179/1465313315Y.0000000017
Dunbar AC, et al. Axenfeld-Rieger Syndrome: a Case Report. J Orthod. 2015;42(4):324-30. PubMed PMID: 26281856.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Axenfeld-Rieger syndrome: a case report. AU - Dunbar,A Craig, AU - McIntyre,Grant T, AU - Laverick,Sean, AU - Stevenson,Brian, Y1 - 2015/08/18/ PY - 2015/8/19/entrez PY - 2015/8/19/pubmed PY - 2018/3/10/medline KW - Axenfeld Rieger syndrome KW - multidisciplinary care KW - orthognathic surgery KW - severe hypodontia SP - 324 EP - 30 JF - Journal of orthodontics JO - J Orthod VL - 42 IS - 4 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. SN - 1465-3133 UR - https://www.unboundmedicine.com/medline/citation/26281856/Axenfeld_Rieger_syndrome:_a_case_report_ L2 - https://journals.sagepub.com/doi/10.1179/1465313315Y.0000000017?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub=pubmed DB - PRIME DP - Unbound Medicine ER -