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양수를 이용한 태아 염색체 분석 1788 예
A Cytogenetic Survey of 1788 Genetic Amniocenteses
문신용(Sin Yong Moon),권경훈(Gyung Hoon Gwon),송남희(Nam Hee Song),설혜원(Hye Won Sul),노미경(Mi Gyung Ro),고희정(Hee Jung Ko),오선경(Sun Gyung Oh),한정호(Jung Ho Han),최규홍(Gyu Hong Choi),김선미(Sun Mi Kim),박중신(Joong Sin Park),전종관(Jong Gwan Jeon),최영민(Young Min Choi),윤보현(Bo Hyun Yoon
UCI I410-ECN-0102-2009-510-005329396

Objective : Amniocentesis is the most prevailing procedures for prenatal cytogenetic analysis. We tried to elucidate the cytogenetic characteristics of amniocentesis performed in the Institute of Reproductive Medicine and Population, Seoul National University and the Department of Obstetrics and Gynecology, Seoul National University Hospital. Methods : From January 1994 to December 1999, transabdominal amniocentesis were performed for cytogenetic analysis in 1738 patients. Results : The most frequent indication for amniocentesis was advanced maternal age(43.4%, 755/1738) and the next was abnormal serum marker(31.7%, 552/1738). The overall incidence of abnormal karyotyping results was 5.4%(97/1788). We showed that the incidence of abnormal karyotyping was different according to its own indication (Pearson chi-square test, p<0.001). Conclusion : The indication for genetic amniocentesis is an important factor to predict anticipated abnormal results.

[자료제공 : 네이버학술정보]
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