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首页> 外文期刊>Taiwanese journal of obstetrics and gynecology >A mullerian anomaly ‘‘without classification’’: Septate uterus with double cervix and longitudinal vaginal septum
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A mullerian anomaly ‘‘without classification’’: Septate uterus with double cervix and longitudinal vaginal septum

机译:苗勒氏畸形“无分类”:子宫分隔,双子宫颈,阴道纵隔

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摘要

The incidence of congenital uterine anomalies in the general population is estimated to be 0.001–10% [1]. The most commonly seen anomalies are septate and arcuate uteri, which represent 75% of all mullerian anomalies. The majority of mullerian duct anomalies are considered to be sporadic or multifactorial in nature; however, polygenic and genetic patterns of inheritance have been described [2], [3].
机译:一般人群中先天性子宫异常的发生率估计为0.001-10%[1]。最常见的异常是分隔的和弓形的子宫,占所有苗勒氏异常的75%。大多数苗勒氏管异常被认为是零星的或多因素的;然而,已经描述了遗传的多基因和遗传模式[2],[3]。

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