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      마판 증후군 소아 환자의 전신마취 하 치과치료 = General Anesthesia for Dental Treatment of a Pediatric Patient with Marfan Syndrome

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      https://www.riss.kr/link?id=A101690811

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      다국어 초록 (Multilingual Abstract)

      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 treatm...

      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 (Reference)

      1 Loeys BL, "The revised Ghent nosology for the Marfan syndrome" 47 : 476-485, 2010

      2 Chan YC, "Ten-year epidmiological review of in-hospital patients with Marfan syndrome" 22 : 608-612, 2008

      3 Singh KK, "TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome" 2006 (2006): 770-777, 2006

      4 De Paepe A, "Revised diagnostic criteria for the Marfan syndrome" 62 : 417-426, 1996

      5 Mizuguchi T, "Recent progress in genetics of Marfan syndrome and Marfan-associated disorders" 52 : 1-12, 2007

      6 Doonquah L, "Oral surgery for patients on anticoagulant therapy: current thoughts on patient management" 56 : 25-41, 2011

      7 Coster PD, "Oral manifestations of patients with Marfan syndrome: A case control study" 93 : 564-572, 2002

      8 Dean JC, "Marfan syndrome: clinical diagnosis and management" 15 : 724-733, 2007

      9 Gray JR, "Marfan syndrome" 33 : 403-408, 1996

      10 Gray JR, "Life expectancy in British Marfan syndrome populations" 54 : 124-128, 1998

      1 Loeys BL, "The revised Ghent nosology for the Marfan syndrome" 47 : 476-485, 2010

      2 Chan YC, "Ten-year epidmiological review of in-hospital patients with Marfan syndrome" 22 : 608-612, 2008

      3 Singh KK, "TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome" 2006 (2006): 770-777, 2006

      4 De Paepe A, "Revised diagnostic criteria for the Marfan syndrome" 62 : 417-426, 1996

      5 Mizuguchi T, "Recent progress in genetics of Marfan syndrome and Marfan-associated disorders" 52 : 1-12, 2007

      6 Doonquah L, "Oral surgery for patients on anticoagulant therapy: current thoughts on patient management" 56 : 25-41, 2011

      7 Coster PD, "Oral manifestations of patients with Marfan syndrome: A case control study" 93 : 564-572, 2002

      8 Dean JC, "Marfan syndrome: clinical diagnosis and management" 15 : 724-733, 2007

      9 Gray JR, "Marfan syndrome" 33 : 403-408, 1996

      10 Gray JR, "Life expectancy in British Marfan syndrome populations" 54 : 124-128, 1998

      11 Faivre L, "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" 123 : 391-398, 2009

      12 Docimo R, "Association between oro-facial defects and systemic alterations in children affected by Marfan syndrome" 7 (7): 700-703, 2013

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-03-09 학술지명변경 한글명 : 대한치과마취과학회지 -> Journal of Dental Anesthesia and Pain Medicine
      외국어명 : Journal of the Korean Dental Society of Anesthesiology -> Journal of Dental Anesthesia and Pain Medicine
      KCI등재
      2015-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2013-01-01 평가 등재후보학술지 유지 (기타) KCI등재후보
      2012-01-01 평가 등재후보 1차 FAIL (기타) KCI등재후보
      2010-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.29 0.29 0.23
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.19 0.18 0.29 0.04
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