Ritvo E R, Ritvo E C, Brothers A M
J Autism Dev Disord. 1982 Jun;12(2):109-14. doi: 10.1007/BF01531303.
The present study is being conducted to explore the hypothesis that genetic and/or congenital factors are etiologically significant in certain persons with the syndrome of autism. To initiate the project, the UCLA Registry for Genetic Studies in Autism was established in 1980. To date 254 families have enrolled. Extensive clinical material and past medical data are being gathered from each family. Information presented in this preliminary report is based solely upon parental reports and prior medical and school evaluations, as the diagnoses have not yet been verified by the authors. Clinical data and family pedigrees will be analyzed by computer-based methods. Blood studies including chromosomes, gene markers, T-cell and B-cell functions, and antibody levels are being conducted on families meeting specific research criteria.
本研究旨在探讨一个假设,即遗传和/或先天性因素在某些自闭症综合征患者中具有病因学意义。为启动该项目,1980年建立了加州大学洛杉矶分校自闭症遗传研究登记处。迄今为止,已有254个家庭登记在册。正在从每个家庭收集广泛的临床资料和既往医疗数据。本初步报告中提供的信息仅基于家长报告以及之前的医疗和学校评估,因为作者尚未对诊断进行核实。临床数据和家系将通过计算机方法进行分析。正在对符合特定研究标准的家庭进行血液研究,包括染色体、基因标记、T细胞和B细胞功能以及抗体水平。