Trounce J Q, Fagan D G, Young I D, Levene M I
Dev Med Child Neurol. 1986 Aug;28(4):467-71. doi: 10.1111/j.1469-8749.1986.tb14284.x.
The cranial ultrasound features of two neonates with neuronal migration disorders are described. One infant had lissencephaly and the other polymicrogyria in conjunction with the Pena-Shokeir syndrome type 1. A third infant is described who was born extremely prematurely and with Down's syndrome, who had similar ultrasound features. By two weeks of age, however, the scan of this third infant had become normal, which illustrates the need for caution in diagnosing migrational disorders in very preterm babies and those with Down's syndrome. The disorders of neuronal migration are discussed.
描述了两名患有神经元迁移障碍的新生儿的头颅超声特征。一名婴儿患有无脑回畸形，另一名患有多小脑回畸形并伴有1型佩纳-肖克综合征。还描述了第三名婴儿，其出生时极度早产且患有唐氏综合征，具有相似的超声特征。然而，到两周大时，第三名婴儿的扫描结果已恢复正常，这表明在诊断极早产儿和唐氏综合征患儿的迁移障碍时需要谨慎。文中讨论了神经元迁移障碍。
