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지원사업
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
- 대한치과마취과학회 Journal of dental anesthesia and pain medicine Journal of dental anesthesia and pain medicine 제13권 제4호
- 발행연도
- 2013.1
- 수록면
- 209 - 214 (6page)
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초록· 키워드
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Multiple caries in a pediatric patient often requires dental treatment under general anesthesia, especially when the patient is suffering from a systemic disease. The patient was a 6-year-old boy with Marfan syndrome and needed extensive dental treatment. Marfan syndrome is an inherited disorder resulting from mutations in Fibrillin-1 gene. Patients are known to have mainly cardiovascular, ocular, and musculoskeletal problems. Although clinical symptoms of the syndrome are age-realted, thus hindering early diagnosis of the disease in young children, our patient had been confirmed by a gene study at a younger age. Medical history of the patient revealed moderate to severe mitral regurgitation and aortic root dilatation, which required mitral valve replacement surgery with a mechanical valve. As a result, the patient was taking warfarin post-operatively and changes in medication had to be made before the dental treatment. Also, prophyalctic antibiotics had to be given before the treatment for prevention of (to prevent the) infective endocarditis. With careful control of the medications and bleeding tendency, general anesthesia and the treatment were done successfully without any complications.
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참고문헌 (12)
참고문헌 신청
Gray JR / 1996 / Marfan syndrome / J Med Genet 33:403~408
De Paepe A / 1996 / Revised diagnostic criteria for the Marfan syndrome / Am J Med Genet 62:417~426
Faivre L / 2009 / Clinical and molecular sudy of 320 children with Marfan Syndrome and related type 1 fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations / Am J Pediatr 123:391~398
Mizuguchi T / 2007 / Recent progress in genetics of Marfan syndrome and Marfan-associated disorders / J Hum Genet 52:1~12
Chan YC / 2008 / Ten-year epidmiological review of in-hospital patients with Marfan syndrome / Ann Vasc Surg 22:608~612
De Paepe A / 1996 / Revised diagnostic criteria for the Marfan syndrome / Am J Med Genet 62:417~426
Faivre L / 2009 / Clinical and molecular sudy of 320 children with Marfan Syndrome and related type 1 fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations / Am J Pediatr 123:391~398
Mizuguchi T / 2007 / Recent progress in genetics of Marfan syndrome and Marfan-associated disorders / J Hum Genet 52:1~12
Chan YC / 2008 / Ten-year epidmiological review of in-hospital patients with Marfan syndrome / Ann Vasc Surg 22:608~612
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