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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 저널정보
- 대한치과보철학회 The Journal of Advanced of Prosthodontics The Journal of Advanced of Prosthodontics 제7권 제5호
- 발행연도
- 2015.1
- 수록면
- 406 - 410 (5page)
이용수
초록· 키워드
오류제보하기
Russell-Silver syndrome (RSS) is a congenital disease characterized by short stature due to growth hormone deficiency, physical asymmetry, inverted triangular face, micrognathia, prominent forehead, and hypodontia. This case report presents a prosthetic management of a 6-year-old patient with Russell-Silver syndrome treated with overdentures on the maxilla and the mandible using the remaining primary teeth. Subsequent and comprehensive dental management considering the growth and development of a young patient will be necessary.
목차
등록된 정보가 없습니다.
참고문헌 (15)
참고문헌 신청
Bergman A / 2003 / Craniofacial morphology and dental age in children with Silver-Russell syndrome / Orthod Craniofac Res 6 : 54 ~ 62
Bhalla G / 2013 / Effect of complete dentures on craniofacial growth of an ectodermal dysplasia patient: a clinical report / J Prosthodont 22 : 495 ~ 500
Cassidy SB / 1986 / Russell-Silver syndrome and hypopituitarism. Patient report and literature review / Am J Dis Child 140 : 155 ~ 159
Cullen CL / 1987 / Russell-Silver syndrome: microdontia and other pertinent oral findings / ASDC J Dent Child 54 : 201 ~ 204
Kotilainen J / 1995 / Craniofacial and dental characteristics of Silver-Russell syndrome / Am J Med Genet 56 : 229 ~ 236
Bhalla G / 2013 / Effect of complete dentures on craniofacial growth of an ectodermal dysplasia patient: a clinical report / J Prosthodont 22 : 495 ~ 500
Cassidy SB / 1986 / Russell-Silver syndrome and hypopituitarism. Patient report and literature review / Am J Dis Child 140 : 155 ~ 159
Cullen CL / 1987 / Russell-Silver syndrome: microdontia and other pertinent oral findings / ASDC J Dent Child 54 : 201 ~ 204
Kotilainen J / 1995 / Craniofacial and dental characteristics of Silver-Russell syndrome / Am J Med Genet 56 : 229 ~ 236
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