Pavone L, Rizzo R, Dobyns W B
Clinica Pediatrica, Università di Catania, Italy.
Childs Nerv Syst. 1993 Nov;9(7):387-90. doi: 10.1007/BF00306189.
Lissencephaly ("smooth brain") is a brain malformation characterized by a smooth cerebral surface, incomplete neuronal migration, and secondary abnormalities such as mental retardation, seizures, and minor facial dysmorphisms. Recent reports have produced evidence supporting several different causes including submicroscopic deletions in chromosome band 17p13.3, autosomal recessive inheritance, intrauterine infection, and intrauterine perfusion failure. We describe the clinical manifestations in seven patients with lissencephaly, and review pertinent studies regarding possible causes. The clinical manifestations were uniformly severe. All patients had severe mental retardation, hypotonia, often combined with spastic paralysis, and infantile spasms which did not respond to treatment. Most had poor growth, postnatal microcephaly, feeding problems, and frequent respiratory infections including pneumonia. None had other significant birth defects. Appropriate studies include computed tomography or magnetic resonance imaging (sometimes both), chromosome analysis, DNA analysis of the lissencephaly region on chromosome 17, electroencephalography and sometimes metabolic studies.
无脑回畸形(“光滑脑”)是一种脑畸形,其特征为脑表面光滑、神经元迁移不完全以及诸如智力迟钝、癫痫发作和轻微面部畸形等继发性异常。最近的报告提供了证据支持几种不同的病因,包括染色体带17p13.3的亚显微缺失、常染色体隐性遗传、宫内感染和宫内灌注衰竭。我们描述了7例无脑回畸形患者的临床表现,并回顾了关于可能病因的相关研究。临床表现均很严重。所有患者都有严重智力迟钝、肌张力减退,常伴有痉挛性瘫痪,以及对治疗无反应的婴儿痉挛症。大多数患者生长发育不良、出生后小头畸形、喂养问题以及包括肺炎在内的频繁呼吸道感染。无一例有其他明显的出生缺陷。适当的检查包括计算机断层扫描或磁共振成像(有时两者都做)、染色体分析、17号染色体上无脑回畸形区域的DNA分析、脑电图检查,有时还包括代谢研究。