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Sirenomelia/mermaid syndrome without imperforate anus in a premature infant

机译:早产儿肛门无穿孔的线虫/美人鱼综合征

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Sirenomelia/mermaid syndrome, which was first described in 1542 and resembled to mermaid because of its characteristic phenotypic appearance, is a very rare congenital anomaly [1]. This disease characterized by the fusion of the lower extremities at different grades, can be accompanied by multiple system anomalies such as musculoskeletal, gastrointestinal system (GIS), genitourinary system (GUS) and cardiovascular system (CVS). The disease is seen in 1/600,000–1000000 rate [1], [2]. In this article, we aimed to present a premature (26 weeks) patient with sirenomelia with very low birth weight (780 g) who could survive postnatal 8 h and had a normal anus, unlike expected in the anomaly.
机译:Sirenomelia /美人鱼综合症是一种非常罕见的先天性异常,最早于1542年被描述,由于其独特的表型外观而类似于美人鱼。该疾病的特征是下肢融合程度不同,可能伴有多个系统异常,例如肌肉骨骼,胃肠系统(GIS),泌尿生殖系统(GUS)和心血管系统(CVS)。该疾病的发生率是1 / 600,000–1000000 [1],[2]。在本文中,我们旨在介绍一名早产(26周),体重很轻(780克)的肺炎线虫病患者,该患者可以在出生后8小时生存,并且肛门正常,这与异常患者的预期不同。

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