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권해석(HS Kuen),박성춘(SC Park),김중근(JG Kim),곽태로(TR Gwag),백옥기(OK Paik) 대한산부인과학회 1985 Obstetrics & Gynecology Science Vol.28 No.6
Cloacal exstrophy is a rare congenital marformation and a distinctive morphologic syndrome. The cardinal clinical features of cloacal exstrohy consist of exstrophy of the bladder, omphalocele, prolapse of the intestine, imperforate anus and lumbosacral myelocele. The essential feature of the syndrome is a failure of cloacal separation at 4~5 weeks of gestation, which results in a persistent cloaca into which the ureter and a rudimentary hindgut open. Most cases of cloacal exstrophy are sporadic, and none has been shown to be genetic in origin. Surgical treatment has been carried with limited effectiveness. The prognosis may be hopeless in a significant number of these infant. Recently we have experienced a case of exstrophy of cloaca in Korea for the first time and we are to report it with brief review of literature.