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Axenfeld-Rieger syndrome: dentofacial manifestation and oral rehabilitation considerations.
Pediatr Dent. 2011 Sep-Oct; 33(5):440-4.PD

Abstract

Axenfeld-Rieger syndrome is a rare genetic disorder characterized by ocular and dental abnormalities. This case demonstrates a comprehensive review of the syndrome's clinical and dental features and describes a case of a 13-year-old boy presenting with it. The patient showed severe hypodontia, microdontia, and short roots. Different treatment options are discussed. Early diagnosis and an interdisciplinary approach are necessary to provide the best short- and long-term treatment plans, as well as treatment and follow-up for individuals with the syndrome.

Authors+Show Affiliations

Barzilai Medical Center, Ashkelon, Israel.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

22104715

Citation

Berenstein-Aizman, Gisela, et al. "Axenfeld-Rieger Syndrome: Dentofacial Manifestation and Oral Rehabilitation Considerations." Pediatric Dentistry, vol. 33, no. 5, 2011, pp. 440-4.
Berenstein-Aizman G, Hazan-Molina H, Drori D, et al. Axenfeld-Rieger syndrome: dentofacial manifestation and oral rehabilitation considerations. Pediatr Dent. 2011;33(5):440-4.
Berenstein-Aizman, G., Hazan-Molina, H., Drori, D., & Aizenbud, D. (2011). Axenfeld-Rieger syndrome: dentofacial manifestation and oral rehabilitation considerations. Pediatric Dentistry, 33(5), 440-4.
Berenstein-Aizman G, et al. Axenfeld-Rieger Syndrome: Dentofacial Manifestation and Oral Rehabilitation Considerations. Pediatr Dent. 2011 Sep-Oct;33(5):440-4. PubMed PMID: 22104715.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Axenfeld-Rieger syndrome: dentofacial manifestation and oral rehabilitation considerations. AU - Berenstein-Aizman,Gisela, AU - Hazan-Molina,Hagai, AU - Drori,Dov, AU - Aizenbud,Dror, PY - 2011/11/23/entrez PY - 2011/11/23/pubmed PY - 2011/12/21/medline SP - 440 EP - 4 JF - Pediatric dentistry JO - Pediatr Dent VL - 33 IS - 5 N2 - Axenfeld-Rieger syndrome is a rare genetic disorder characterized by ocular and dental abnormalities. This case demonstrates a comprehensive review of the syndrome's clinical and dental features and describes a case of a 13-year-old boy presenting with it. The patient showed severe hypodontia, microdontia, and short roots. Different treatment options are discussed. Early diagnosis and an interdisciplinary approach are necessary to provide the best short- and long-term treatment plans, as well as treatment and follow-up for individuals with the syndrome. SN - 0164-1263 UR - https://www.unboundmedicine.com/medline/citation/22104715/Axenfeld_Rieger_syndrome:_dentofacial_manifestation_and_oral_rehabilitation_considerations_ L2 - https://www.ingentaconnect.com/openurl?genre=article&issn=0164-1263&volume=33&issue=5&spage=440&aulast=Berenstein-Aizman DB - PRIME DP - Unbound Medicine ER -