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独眼畸形13三体综合征的颞骨表现。

Temporal bone findings in trisomy 13 with cyclopia.

作者信息

Tomoda K, Shea J J, Shenefelt R E, Wilroy R S

出版信息

Arch Otolaryngol. 1983 Aug;109(8):553-8. doi: 10.1001/archotol.1983.00800220059015.

Abstract

Temporal bone findings in a fetus with trisomy 13 syndrome and cyclopia may be histopathologically characterized by the dysplasia of bony and membranous labyrinth and of the nervous system. In the left ear, there was a shortened cochlea housing a malformed Corti's organ appearing as a ribbonlike structure, an unexpected canal running obliquely through the scala tympani, a peculiar shape of the utricular macula and posterior canal crista, and a delayed ossifying process in the otic capsule. The poor development of the structures in the seventh and eighth nerves and their ganglions was observed in both ears. The type of anomaly can be classified as Mondini or Mondini-Alexander. The several anomalies might involve the organs that begin to develop during the period from five to eight gestational weeks.

摘要

患有13三体综合征和独眼畸形胎儿的颞骨组织病理学表现可能为骨迷路、膜迷路及神经系统发育异常。左耳可见耳蜗缩短,其中柯蒂器畸形,呈带状结构;一条意外的管道斜穿鼓阶;椭圆囊斑和后半规管嵴形状奇特;耳囊骨化过程延迟。双耳均观察到第Ⅶ和第Ⅷ神经及其神经节结构发育不良。这种异常类型可归类为蒙迪尼型或蒙迪尼-亚历山大型。这些异常可能累及在孕5至8周期间开始发育的器官。

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