Pauls D L
Child Study Center, Yale University School of Medicine, 230 South Frontage Road, New Haven, CT 06520, USA.
Curr Psychiatry Rep. 2001 Apr;3(2):152-7. doi: 10.1007/s11920-001-0013-2.
Twin and family studies demonstrate that Tourette syndrome (TS) is a genetic disorder. Early segregation analyses of family data were consistent with the hypothesis of autosomal dominant transmission; however, more recent studies suggest that the mode of inheritance is more complex. Current findings suggest that there are genes of major effect with other genes acting as modifiers. Several genome scans have been completed and several regions of interest have been identified that may harbor susceptibility genes for TS. Work is currently underway to replicate and extend these initial results.
双胞胎和家族研究表明,妥瑞氏症(TS)是一种遗传性疾病。对家族数据的早期分离分析与常染色体显性遗传的假设一致;然而,最近的研究表明,遗传模式更为复杂。目前的研究结果表明,存在起主要作用的基因,其他基因则作为修饰基因。已经完成了几项全基因组扫描,并确定了几个可能含有妥瑞氏症易感基因的感兴趣区域。目前正在开展工作以复制和扩展这些初步结果。