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
- 저널정보
- 대한치과마취과학회 Journal of dental anesthesia and pain medicine Journal of dental anesthesia and pain medicine 제13권 제1호
- 발행연도
- 2013.1
- 수록면
- 13 - 18 (6page)
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초록· 키워드
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CATCH 22 syndrome is a one of the most common chromosome microdeletion syndrome with multiple organ anomalies in humans, with an incidence of approximately 1:4,000 to 1:5,000 live births. It is caused by a microdeletion of 1.5 to 3.0 megabases on the long arm of chromosome 22. The phenotypic spectrum of this disorder is wide and various. A 19-year-old patient who showed delayed growth and development (Height; 110 cm, Weight; 18 kg) was referred to our department for the treatment of dental cavities. She was diagnosed as CATCH 22 syndrome in 2004. Physical examination revealed hypertelorism, a short philtrum, thick reflected lips and a small mouth. She underwent cleft palate surgery at 1 year of age and heart valve surgery due to the cardiovascular abnormality at 13 years of age. Convulsive seizures had persisted until 5 years ago but are well controlled at present. Oral examination showed poor oral hygiene, crowding, prolonged retention on #65, 75 and dental cavities on #16, 21, 65, 26, 36, and 46. Cavity treatment and prophylaxis were performed under general anesthesia. Also continuous follow-up checks have been carrying out with the periodic prophylaxis and dental home education. Problems with numerous cavities and gingivitis which can lead to specific risks are common for CATCH 22 syndrome patients. It is therefore of great importance that these patients are referred to foremost physician and dental specialist for the oral care. In addition, preventive treatment targeting the risk of dental cavities and gingivitis is especially important and, as the syndrome involves many different medical problems, the dental treatment should be carried out in collaboration with the patient's physician.
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참고문헌 (12)
참고문헌 신청
Okan Toka / 2010 / Dental aspects in patients with DiGeorge syndrome / Quintessence international 41(7):551~557
Burn J / 1993 / Conotruncal anomaly face syndrome 22q11 / J Med Genet 30:822~824
Steven A / 1990 / Digeorge syndrome and velocadiofacial syndrome / Pediatrics 85:530~536
Klingberg G / 2002 / Oral manifestations in 22q11 deletion syndrome / Int J paediatric dentistry 12(1):14~23
Motzkin B / 1993 / Variable phenotypes in velocardiofacial syndrome with chromosomal deletion / J pediatric dentistry 123(3):406~410
Burn J / 1993 / Conotruncal anomaly face syndrome 22q11 / J Med Genet 30:822~824
Steven A / 1990 / Digeorge syndrome and velocadiofacial syndrome / Pediatrics 85:530~536
Klingberg G / 2002 / Oral manifestations in 22q11 deletion syndrome / Int J paediatric dentistry 12(1):14~23
Motzkin B / 1993 / Variable phenotypes in velocardiofacial syndrome with chromosomal deletion / J pediatric dentistry 123(3):406~410
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