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Sirenomelia dipus in a dizygotic twin

机译:同卵双胞胎中的Sirenomelia dipus

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摘要

A rare case of sirenomelia in a LBW, IUGR & second of a dizygotic twin having multiple congenital anomalies is being reported. Apart from the features of sirenomelia, the newborn had a single umbilical artery, radial hypoplasia, total anorectal & urogenital agenesis and undetermined sex. The single umbilical artery had a normal origin from the iliac artery. There was no Vitelline arterial steal phenomenon. Theories put forward regarding etiopathogenesis are discussed. We conclude that the anomalies in the present case are difficult to be explained with earlier proposed theories. This puts an emphasis on reconsideration of old theory of genetic injury to the embryo by unknown factors.
机译:据报道,LBW,IUGR和第二个同卵双生双胞胎中有多个先天性异常的少见的蛛网膜病例。除了小隔尿膜炎的特征外,新生儿还具有单条脐动脉,radial骨发育不全,整个肛门直肠和泌尿生殖器发育不全以及性别未定。单条脐动脉起源于artery动脉。没有Vitelline的动脉盗窃现象。讨论了有关病因的提出的理论。我们得出结论,当前情况下的异常很难用较早提出的理论来解释。这强调了对未知因素对胚胎遗传损伤的古老理论的重新考虑。

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