Department of Neuroscience, Paediatric Neurology Unit, "Tor Vergata" University of Rome, Italy.
Ital J Pediatr. 2010 Feb 14;36:17. doi: 10.1186/1824-7288-36-17.
Mental retardation is a heterogeneous condition, affecting 1-3% of general population. In the last few years, several emerging clinical entities have been described, due to the advent of newest genetic techniques, such as array Comparative Genomic Hybridization. The detection of cryptic microdeletion/microduplication abnormalities has allowed genotype-phenotype correlations, delineating recognizable syndromic conditions that are herein reviewed. With the aim to provide to Paediatricians a combined clinical and genetic approach to the child with cognitive impairment, a practical diagnostic algorithm is also illustrated. The use of microarray platforms has further reduced the percentage of "idiopathic" forms of mental retardation, previously accounted for about half of total cases. We discussed the putative pathways at the basis of remaining "pure idiopathic" forms of mental retardation, highlighting possible environmental and epigenetic mechanisms as causes of altered cognition.
智力障碍是一种异质性疾病,影响一般人群的 1-3%。在过去的几年中,由于最新的遗传技术(如阵列比较基因组杂交)的出现,已经描述了几种新兴的临床实体。隐匿性微缺失/微重复异常的检测使得基因型-表型相关性得以确定,划定了可识别的综合征状态,本文对此进行了综述。为了为儿科医生提供一种针对认知障碍儿童的综合临床和遗传方法,还说明了一种实用的诊断算法。微阵列平台的使用进一步降低了以前约占总病例一半的“特发性”智力障碍的比例。我们讨论了基础上剩余的“纯特发性”智力障碍形式的可能途径,强调了可能的环境和表观遗传机制是导致认知改变的原因。