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首页> 外文期刊>Case Reports in Obstetrics and Gynecology >A Case of Type I Sirenomelia Complicated by Severe Oligohydramnios in the First Trimester
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A Case of Type I Sirenomelia Complicated by Severe Oligohydramnios in the First Trimester

机译：在孕中期的严重寡核苷酸复杂的I型Sirenomelia的情况

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摘要

Sirenomelia is a very rare congenital anomaly. Type I is the mildest type, and the long bone structures are all normally present with only soft tissue fusion. We experienced a case of type I sirenomelia complicated by severe oligohydramnios. Because of severe oligohydramnios, ultrasonographic images were not very clear. The associated findings with sirenomelia (single umbilical artery and bilateral renal agenesis) were helpful for the prenatal diagnosis of this disease. Detailed sonographic examination of the fetus was thought to be necessary for the accurate prenatal diagnosis of sirenomelia.
机译：西列伦洛尼亚是一个非常罕见的先天性异常。 I型是最温和的类型，并且长骨结构通常存在，只有软组织融合。我们经历了一种由严重的寡少米斯复杂的I型Sirenomelia的情况。由于严重的寡少数，超声图像不是很清楚。 Sirenomelia的相关结果（单脐动脉和双侧肾功能衰退）有助于对该疾病的产前诊断。对胎儿的详细超声检查被认为是Sirenomelia的准确产前诊断所必需的。

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