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首页> 外文期刊>International Journal of Reproduction, Contraception, Obstetrics and Gynecology >A rare case of conjoined twins presenting as dicephalus parapagus: a case report
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A rare case of conjoined twins presenting as dicephalus parapagus: a case report

机译:罕见的双胞胎双胞胎表现为副头畸形:病例报告

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Conjoined twinning is a congenital abnormality resulting in various presentations of the fetuses in utero. It is a rare embryological developmental disorder occurring in one in 100,000 births. We present a case of conjoined twinning, which is characterized by the presence of two heads, single vertebral column and single symphysis pubis, with single genitor-urinary tract and single gastro intestinal tract. The present condition, referred to as dicephalus parapagus, is a rare entity among the conjoined twinning and has seldom positive outcomes. The mechanism of occurrence of conjoined twinning has been proposed either through fusion or fission of the embryos. In either case, surgical separation of the conjoined twins is often unsuccessful and results in increased morbidity and mortality. However, it is essential to screen for the presence of such congenital anomalies early during pregnancy, in order to terminate and provide parental counselling.
机译:连生双胞胎是先天性异常,导致子宫内胎儿的各种表现。这是一种罕见的胚胎发育障碍,每十万分之一出生。我们介绍了一个联合孪生的病例,其特征是存在两个头部,单个椎骨柱和单个耻骨联合,单个生殖泌尿道和单个胃肠道。目前的状况,被称为“ paraparaus parapagus”,是联结双胞胎中罕见的个体,很少有阳性结果。通过胚胎的融合或裂变已经提出了发生连环孪生的机制。在这两种情况下,连体双胞胎的手术分离通常都不成功,并导致发病率和死亡率增加。但是,必须在妊娠早期筛查此类先天性异常的存在,以终止并提供父母咨询。

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