Simma B, Felber S, Maurer H, Gassner I, Krassnitzer S
University Clinics of Pediatrics, University of Innsbruck, Austria.
Pediatr Radiol. 1990;20(7):554-5. doi: 10.1007/BF02011390.
We report on a boy with type II lissencephaly and congenital muscular dystrophy. The patient presented with the features of a cerebro-oculo-muscular syndrome (COMS). We describe the clinical presentations and the characteristic sonographic and MR findings.
我们报告了一名患有II型无脑回畸形和先天性肌营养不良的男孩。该患者表现出脑眼肌综合征（COMS）的特征。我们描述了其临床表现以及特征性的超声和磁共振成像（MR）表现。
