Browse

증례 보고 : Rieger syndrome

DC Field Value Language
dc.contributor.author이홍모-
dc.contributor.author김정욱-
dc.contributor.author장기택-
dc.contributor.author이상훈-
dc.contributor.author한세현-
dc.contributor.author김종철-
dc.date.accessioned2010-02-01T09:52:39Z-
dc.date.available2010-02-01T09:52:39Z-
dc.date.issued2003-
dc.identifier.citation대한소아치과학회지, 30:667-672, 2003.en
dc.identifier.issn1226-8496-
dc.identifier.urihttps://hdl.handle.net/10371/47823-
dc.description.abstractRieger 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.en
dc.language.isokoen
dc.publisher대한소아치과학회en
dc.subjectRieger syndromeen
dc.subjectHypodontiaen
dc.subjectPolycoriaen
dc.subjectPosterior embryotoxonen
dc.subjectMaxillary hypoplasiaen
dc.title증례 보고 : Rieger syndromeen
dc.typeArticleen
dc.contributor.AlternativeAuthorLee, Hong-Mo-
dc.contributor.AlternativeAuthorKim, Jung-Wook-
dc.contributor.AlternativeAuthorJang, Ki-Taeg-
dc.contributor.AlternativeAuthorLee, Sang-Hoon-
dc.contributor.AlternativeAuthorHahn, Se-Hyun-
dc.contributor.AlternativeAuthorKim, Chong-Chul-
Appears in Collections:
College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Journal Papers (저널논문_치의학과)
Files in This Item:
  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse