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임신부에게 항부정맥제를 투여하여 치유된 태아복수를 동반한 태아 상실성 빈맥증
신병식 ( Byoung Shick Shin ),조용 ( Yong Cho ),노의선 ( Eu Sun Ro ),이동욱 ( Dong Ook Lee ),문기숙 ( Ki Suk Mun ) 대한산부인과학회 2004 Obstetrics & Gynecology Science Vol.47 No.9
We experienced a case of fetal supraventricular tachycardia (SVT) with fetal ascites diagnosed at 29 weeks of gestation in 29 year-old primigravida woman. Transplacental fetal therapy with maternal oral antiarrhythmic agent (verapamil, diltiazem) resulted
나연화(Yeon Hwa La),신병식(Byoung Shick Shin),박영하(Young Hwa Park),금형용(Hyung Yong Keum),김종철(Zong Chul Kim),이동욱(Dong Ook Lee),정우철(Woo Chuel Jung),이성원(Sung Won Lee),조용(Yong Cho),노의선(Eu Sun Ro) 대한산부인과학회 2001 Obstetrics & Gynecology Science Vol.44 No.11
Trisomy 18, called Edward syndrome, occurs in about 3500-8000 births. It is much more common at conception, with about 95% of cases resulting in spontaneous abortion or stillbirth. Postnatal survival is poor, with the majority of patients dying in early infancy. Characteristic findings include cardiac malformations, mental retardation, growth retardation, a prominent occiput, micrognathia, clenched hands, and rocker-bottom feet, omphalocele. The prenatal sonographic findings of our case include delayed growth, omphalocele, wrist joint fixation, choroid plexus cyst, hydramnios and postnatal gross findings include growth retardation, omphalocele, wirst joint fixation, absence of radius, syndactyly, focal absence of phalanges and flexion deformities of fingers and toes. We report a case of prenatally diagnosed Edward syndrome, which is confirmed by chromosome analysis, with brief review of related literatures.