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증례 보고 : Russell-Silver Syndrome

DC Field Value Language
dc.contributor.author이진-
dc.contributor.author장기택-
dc.contributor.author김종철-
dc.date.accessioned2010-02-01T10:00:24Z-
dc.date.available2010-02-01T10:00:24Z-
dc.date.issued2002-
dc.identifier.citation대한소아치과학회지 29:51-56, 2002.en
dc.identifier.issn1226-8496-
dc.identifier.urihttps://hdl.handle.net/10371/47979-
dc.description.abstractRussell-Silver syndrome is a type of intrauterine growth retardation, characterized by short stature noted at birth, hemiatrophy or asymmetry, variation in sexual development and other abnormalities, including cafe-aulait pigmentation and clinodactyly. Facial features commonly associated with this syndrome are a small triangular face, decreased facial height, down-turned corners of the mouth(shark's mouth), a small mandible, and occasionally asymmetry. The major intra-oral features of the syndrome that have been reported are a high-arched palate, delayed tooth eruption, microdontia, hypodontia, and crowding. These cases were diagnosed at birth as Russell-Silver syndrome by clinical features such as prenatal growth retardation, short stature, low body weight, et al., and have been treated with growth hormone. The purpose of this paper is to report the dental findings of two patients and review the pertinent literature through the two cases.en
dc.language.isokoen
dc.publisher대한소아치과학회en
dc.subjectGrowth retardationen
dc.subjectClinodactylyen
dc.subjectAsymmetryen
dc.subjectShark's mouthen
dc.subjectCrowdingen
dc.title증례 보고 : Russell-Silver Syndromeen
dc.typeArticleen
dc.contributor.AlternativeAuthorLee, Jin-
dc.contributor.AlternativeAuthorJang, Ki-Taeg-
dc.contributor.AlternativeAuthorKim, Chong-Chul-
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