Cornelia de Lange syndrom 환아에서 발생한 Incomplete cleft palate의 치험례

Incomplete cleft palate related to Cornelia de Lange syndrome -A case report-

  • 윤보근 (전북대학교 치과대학 구강악안면외과학교실 및 구강생체과학연구소) ;
  • 이환수 (전북대학교 치과대학 구강악안면외과학교실 및 구강생체과학연구소) ;
  • 신효근 (전북대학교 치과대학 구강악안면외과학교실 및 구강생체과학연구소)
  • Yoon, Bo-Keun (Dept. of Oral and Maxillofacial surgery, School of Dentistry, Institute of Oral Bio-Science, ChonBuk National University) ;
  • Lee, Hwan-Soo (Dept. of Oral and Maxillofacial surgery, School of Dentistry, Institute of Oral Bio-Science, ChonBuk National University) ;
  • Shin, Hyo-Keun (Dept. of Oral and Maxillofacial surgery, School of Dentistry, Institute of Oral Bio-Science, ChonBuk National University)
  • 발행 : 2000.06.30

초록

Cornelia de Lange syndrome is a disorder of unknown biochemical and geneic basis that is recognized on the basis of characteristic facies(low anterior hairline, synophrys, anteverted nares, maxillary prognathism, long philtrum, carp mouth) in association with prenatal and postnatal growth retardation, mental retardation and, in many cases, upper limb anomalies. We treated the patient with incomplete cleft palate related to Cornelia de Lange syndrome.

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