권호기사보기
기사명 | 저자명 | 페이지 | 원문 | 기사목차 |
---|
대표형(전거형, Authority) | 생물정보 | 이형(異形, Variant) | 소속 | 직위 | 직업 | 활동분야 | 주기 | 서지 | |
---|---|---|---|---|---|---|---|---|---|
연구/단체명을 입력해주세요. |
|
|
|
|
|
* 주제를 선택하시면 검색 상세로 이동합니다.
Floating Harbor 증후군 (FHS)은 드문 유전질환이다. 본 증례는 FHS를 가진 환아에 대해 소개하였다. 환아는 독특한 얼굴 형태, 저성장된 상악과 전돌된 하악을 동반한 심한 골격적 3급 부정교합, 결손치, 왜소치, 상악 치아의 이소맹출을 보였다. 쌍둥이 여동생은 하악전돌을 동반한 경미한 골격성 3급 부정교합은 보였으나 결손치와 왜소치는 보이지 않았다. 높은 구개궁, 넓은 난형의 하악궁에 비해 좁은 V형의 상악궁, 역의 관계의 상하악 구치간 폭경으로 인한 구치부 반대교합이 환자의 모델 분석을 통해 확인되었다. 이러한 특성은 쌍둥이에서는 나타나지 않았다. 행동면에서 환아는 경미한 정신지체로 인해 치과 치료 중 낮은 협조도를 보였다.
Floating-Harbor syndrome (FHS) is a rare genetic disorder. This report introduced in a patient with FHS. Distinctive facial characteristics, severe skeletal class 3 malocclusion with underdeveloped maxilla and protruded mandible, congenital missing teeth, microdontia and ectopic positions of maxillary teeth were presented in the patient. In his twin sister, mild skeletal class 3 malocclusion with protruded mandible was observed but congenital missing teeth and microdontia were not observed. High-arched palate, narrow V-shaped maxillary arch compared to wide and ovoid mandibular arch and inverse relationship between the maxillary and mandibular intermolar width resulted in posterior crossbite were confirmed by model analysis of the patient. These were not observed in the twins. Behaviorally, poor cooperation during dental treatment because of mental retardation was observed in the patient.
번호 | 참고문헌 | 국회도서관 소장유무 |
---|---|---|
1 | Nikkel SM, Dauber A, Boycott KM, et al . : The phenotype of Floating-Harbor syndrome: clinical characterization of 52individuals with mutations in exon 34 of SRCAP. Orphanet J Rare Dis , 8:1-9, 2013. | 미소장 |
2 | Kehrer M, Beckmann A, Tzschach A, et al . : Floating-Harbor syndrome: SRCAP mutations are not restricted to exon 34. Clin Genet , 85:498-499, 2013. | 미소장 |
3 | Seifert W, Meinecke P, Horn D, et al . : Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome. BMC Med Genet , 15:1-5, 2014. | 미소장 |
4 | Hood RL, Lines MA, FORGE Canada Consortium, et al . :Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome. Am J Hum Genet , 90:308-313, 2012. | 미소장 |
5 | Budisteanu M, Bögershausen N, Wollnik B, et al . : Floating-Harbor syndrome: presentation of the first Romanian patient with a SRCAP mutation and review of the literature. Balkan J Med Genet , 21:83-86, 2018. | 미소장 |
6 | Messina G, Atterrato MT, Dimitri P : When chromatin organisation floats astray: the Srcap gene and Floating-Harbor syndrome. J Med Genet , 53:793-797, 2016. | 미소장 |
7 | White SM, Morgan A, Hurst JA, et al . : The phenotype of Floating-Harbor syndrome in 10 patients. Am J Med Genet A , 152:821-829, 2010. | 미소장 |
8 | Bastaki L, El-Nabi MM, Naguib KK, et al . : Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review. East Mediterr Health J , 13:975-979, 2007. | 미소장 |
9 | Arpin S, Afenjar A, Héron D, et al . : Floating-Harbor Syndrome:report on a case in a mother and daughter, further evidence of autosomal dominant inheritance. Clin Dysmorphol , 21:11-14, 2012. | 미소장 |
10 | Zhang S, Chen S, Shen Y, et al . : Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome. Orphanet J Rare Dis , 14:1-11, 2019. | 미소장 |
11 | De Benedetto MS, Mendes FM, Ciamponi AL, et al . : Floating-Harbor Syndrome: case report and craniofacial phenotype characterization. Int J Paediatr Dent , 14:208-213, 2004. | 미소장 |
12 | Houlston RS, Collins AL, Dennis NR, Temple IK : Further observations on the Floating-Harbor syndrome. Clin Dysmorphol , 3:143-149, 1994. | 미소장 |
13 | Majewski F, Lenard HG : The Floating-Harbor syndrome. Eur J Pediatr, 150:250-252, 1991. | 미소장 |
14 | Singh A, Bhatia HP, Mohan A, et al . : A novel finding of oligodontia and ankyloglossia in a 14-year-old with Floating-Harbor syndrome. Spec Care Dentist , 37:318-321, 2017. | 미소장 |
15 | Ala-Mello S, Peippo M : Two more diagnostic signs in the Floating-Harbor syndrome. Clin Dysmorphol , 5:85-88, 1996. | 미소장 |
16 | Ala-Mello S, Peippo M : The first Finnish patient with the Floating-Harbor syndrome: the follow-up of eight years. Am J Med Genet , 130:317-319, 2004. | 미소장 |
17 | Smeets E, Fryns JP, Van den Berghe H : The Floating-Harbor syndrome: report of another patient and differential diagnosis with Shprintzen syndrome. Genet Couns, 7:143-146, 1996. | 미소장 |
18 | Midro AT, Olchowik B, Wiśniewski A : Floating Harbor syndrome. Case report and further syndrome delineation. Ann Genet, 40:133-138, 1997. | 미소장 |
19 | Choi EM, Lee DH, Jang JH, et al . : The first Korean case with Floating-Harbor syndrome with a novel SRCAP mutation diagnosed by targeted exome sequencing. Korean J Pediatr, 61:403-406, 2018. | 미소장 |
20 | Bamshad, Michael J, Shendure J, et al . : Exome sequencing as a tool for Mendelian disease gene discovery. Nat Rev Genet , 12:745-755, 2011. | 미소장 |
21 | Amita M, Srivastava P, Agarwal D, Phadke SR : Floating harbor syndrome. Indian J Pediatr , 83:896-897, 2016. | 미소장 |
22 | Karaer K, Karaoguz MY, Percin EF, et al . : Floating-Harbor syndrome: A first female Turkish patient? Genet Couns , 17:465-468, 2006. | 미소장 |
23 | Paluzzi A, Viva LJ, Patton MA, et al . : Ruptured cerebral aneurysm in a patient with Floating-Harbor syndrome. Clin Dysmorphol, 17:283-285, 2008. | 미소장 |
24 | Dempsey PJ, Townsend GC : Genetic and environmental contributions to variation in human tooth size. Heredity (Edinb) , 86:685-693, 2001. | 미소장 |
*표시는 필수 입력사항입니다.
*전화번호 | ※ '-' 없이 휴대폰번호를 입력하세요 |
---|
기사명 | 저자명 | 페이지 | 원문 | 기사목차 |
---|
번호 | 발행일자 | 권호명 | 제본정보 | 자료실 | 원문 | 신청 페이지 |
---|
도서위치안내: 정기간행물실(524호) / 서가번호: 국내03
2021년 이전 정기간행물은 온라인 신청(원문 구축 자료는 원문 이용)
우편복사 목록담기를 완료하였습니다.
*표시는 필수 입력사항입니다.
저장 되었습니다.