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The Rieger syndrome: orofacial manifestations. Case report of a rare condition.
Quintessence Int. 2003 Oct; 34(9):689-92.QI

Abstract

Rieger syndrome is a rare, autosomal dominant disorder due to developmental arrest of tissues derived from neural crest ectoderm in the third trimester. It is characterized by abnormalities of the anterior chamber of the eye coincident with dental and craniofacial anomalies. Early recognition of dental anomalies aids in detection of the syndrome and prevents progressive loss of vision. This case report discusses the ocular, dental, and craniofacial findings and the overall management of the patient.

Authors+Show Affiliations

Department of Dentistry, Government Medical and College Hospital, Chandigarh, India.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

14982223

Citation

Singh, Jagjit, et al. "The Rieger Syndrome: Orofacial Manifestations. Case Report of a Rare Condition." Quintessence International (Berlin, Germany : 1985), vol. 34, no. 9, 2003, pp. 689-92.
Singh J, Pannu K, Lehl G. The Rieger syndrome: orofacial manifestations. Case report of a rare condition. Quintessence Int. 2003;34(9):689-92.
Singh, J., Pannu, K., & Lehl, G. (2003). The Rieger syndrome: orofacial manifestations. Case report of a rare condition. Quintessence International (Berlin, Germany : 1985), 34(9), 689-92.
Singh J, Pannu K, Lehl G. The Rieger Syndrome: Orofacial Manifestations. Case Report of a Rare Condition. Quintessence Int. 2003;34(9):689-92. PubMed PMID: 14982223.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The Rieger syndrome: orofacial manifestations. Case report of a rare condition. AU - Singh,Jagjit, AU - Pannu,Karneev, AU - Lehl,Gurvanit, PY - 2004/2/26/pubmed PY - 2004/3/18/medline PY - 2004/2/26/entrez SP - 689 EP - 92 JF - Quintessence international (Berlin, Germany : 1985) JO - Quintessence Int VL - 34 IS - 9 N2 - Rieger syndrome is a rare, autosomal dominant disorder due to developmental arrest of tissues derived from neural crest ectoderm in the third trimester. It is characterized by abnormalities of the anterior chamber of the eye coincident with dental and craniofacial anomalies. Early recognition of dental anomalies aids in detection of the syndrome and prevents progressive loss of vision. This case report discusses the ocular, dental, and craniofacial findings and the overall management of the patient. SN - 0033-6572 UR - https://www.unboundmedicine.com/medline/citation/14982223/The_Rieger_syndrome:_orofacial_manifestations__Case_report_of_a_rare_condition_ L2 - http://www.diseaseinfosearch.org/result/6329 DB - PRIME DP - Unbound Medicine ER -