Prenatal diagnosis of an XY fetus with aphallia and cloacal exstrophy variant.
Prenatal diagnosis of an XY fetus with aphallia and cloacal exstrophy variant.
复制标题
患有无阴茎和泄殖腔外翻变异的 XY 胎儿的产前诊断。
DOI：
10.7863/jum.1994.13.4.323
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发表时间：
1994
影响因子：
2.3
通讯作者：
J. Mandell
中科院分区：
文献类型：
--
作者：
M. Carr;B. Benacerraf;J. Mandell
A 29 year old gravida 1 woman underwent ultrasono• graphic evaluation at 26 weeks' gestation. Examination of the fetal genitalia revealed a normal scrotum and testes with no phallus present (Fig. 1). The kidneys appeared normal; however, no bladder was visualized. An omphalocele was present with a low insertion of the umbilical cord (Fig. 2). Amniotic fluid volume was normal. The differential diagnosis included bladder exstrophy with aphallia versus a cloacal variant, and plans were made to effect delivery at a tertiary care center. The 2400 g infant was born by spontaneous vaginal delivery at 35 weeks' gestation with Apgar scores of 9 and 9. Abnormalities on physical examination included an omphalocele, a meconium stained umbilical cord that was markedly ectatic (Fig. 3), a bifid scrotum with palpable
