지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2018.1
- 수록면
- 115 - 122 (8page)
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초록· 키워드
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Noonan syndrome is characterized by distinctive facial features, short stature, and congenital heart disease. It is a congenital genetic disorder with a prevalence of between 1/1,000 and 1/2,500 in both genders. An 11-year-old boy with Noonan syndrome visited the hospital with an ectopically positioned tooth. A pulmonary stenosis was diagnosed and his growth and development were delayed. In many cases of this diseases there is obvious hemostasis, which he was not experiencing. His facial appearance showed characteristic features of Noonan syndrome. The patient showed a dental class II relationship, labioversion of the upper anterior teeth, and a shallow overbite. Radiographic examination revealed that the upper right canine was ectopically positioned, which led to root resorption of the upper right lateral incisor. A lateral cephalometric radiograph revealed a craniofacial pattern that was within normal limits. Surgical opening and button attachment on the impacted upper right canine were performed and traction was applied on the impacted tooth using a removable appliance. This patient was mildly affected by Noonan syndrome and showed some dental problems. However, few studies have reported the oral characteristics of Noonan syndrome despite its high incidence. Thus, this case report describes the oral features and management of Noonan syndrome.
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참고문헌 (16)
참고문헌 신청
Romano AA / 2010 / Noonan syndrome : clinical features, diagnosis, and management guidelines / Pediatrics 126:746~759
Mendez HM / 1985 / Noonan syndrome : a review / Am J Med Genet 21:493~506
Mallineni SK / 2014 / Oral manifestations of Noonan syndrome: review of the literature and a report of four cases / Rom J Morphol Embryol 55:1503~1509
Barberia LE / 2003 / Etiopathogenic analysis of the caries on three patients with Noonan Syndrome / Med Oral 8:136~142
Martinez-Quintana E / 2012 / LEOPARD Syndrome : Clinical Features and Gene Mutations / Mol Syndromol 3:145~157
Mendez HM / 1985 / Noonan syndrome : a review / Am J Med Genet 21:493~506
Mallineni SK / 2014 / Oral manifestations of Noonan syndrome: review of the literature and a report of four cases / Rom J Morphol Embryol 55:1503~1509
Barberia LE / 2003 / Etiopathogenic analysis of the caries on three patients with Noonan Syndrome / Med Oral 8:136~142
Martinez-Quintana E / 2012 / LEOPARD Syndrome : Clinical Features and Gene Mutations / Mol Syndromol 3:145~157
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