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증례 보고 : Rieger syndrome

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Authors
이홍모; 김정욱; 장기택; 이상훈; 한세현; 김종철
Issue Date
2003
Publisher
대한소아치과학회
Citation
대한소아치과학회지, 30:667-672, 2003.
Keywords
Rieger syndromeHypodontiaPolycoriaPosterior embryotoxonMaxillary hypoplasia
Abstract
Rieger syndrome is a rare, autosomal dominant genetic disorder characterized by malformation of the anterior chamber of the eye(goniodysgenesis) coincident with hypodontia. It may also be accompanied by a spectrum of dental, craniofacial and somatic anomalies. Mutations in paired-like homeodomain transcription factor2(PITX2) are associated with the syndrome, and its frequency in the general population has been estimated to be 1 : 200,000. In the present case, the patient, 4 year 7 month-old female, had posterior embryotoxon and polycoria. The maxilla was retrusive in cephalometric radiography. She had congenital missing on #52, #62 and some tooth germs of permanent tooth were not detected in panoramic radiography. The purpose of this paper is to report the dental and craniofacial findings and review the pertinent literature through this case.
ISSN
1226-8496
Language
Korean
URI
https://hdl.handle.net/10371/47823
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College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Journal Papers (저널논문_치의학과)
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