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대한산부인과초음파학회지 제14권 제1호 2012년
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배꼽탈장이 동반된 13번 염색체 전좌에 의한 파타우 증후군

경희대학교 의학전문대학원 산부인과학교실
정효주, 권병수, 박지영, 편승연, 동서연, 설현주, 정의, 김승보


A Case of Patau Syndrome with Robertsonian Translocation (13;13)(q10;q10) Presenting with Isolated Omphalocele

Hyo Joo Jeong, Byung Su Kwon, Ji Young Park, Seung Yeon Pyeon, Seo-Yun Tong, Hyun-Joo Seol, Eui Jung, Seung Bo Kim,
Department of Obstetrics and Gynecology, College of Medicine, Kyung Hee University, Seoul, Korea

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Patau syndrome (trisomy 13) is usually associated with multiple malformations such as facial defect, skeletal anomalies, cardiac defect, midline anomalies and severe mental retardation. Sonographic evaluation of structural anomalies is useful to enable prenatal diagnosis of Patau syndrome, which is less detected in maternal serum screening. Although major structural anomalies would be easily detected on prenatal ultrasound, some abnormalities are subtle and result in late gestational age at diagnosis. Here we report a case of Patau syndrome with Robertsonian translocation, (13;13)(q10;q10) presenting with isolated omphalocele, which was detected at the third trimester.

  • Key Word : Patau syndrome, Trisomy 13, Robertsonian translocation, Omphalocele
  • 교신 저자 : seolhj@khu.ac.kr
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