Prontera Paolo, Serino Domenico, Caldini Bernardo, Scarponi Laura, Merla Giuseppe, Testa Giuseppe, Muti Marco, Napolioni Valerio, Mazzotta Giovanni, Piccirilli Massimo, Donti Emilio
Medical Genetics Unit, Hospital "S. M. della Misericordia", University of Perugia, Via E. dal Pozzo, 06123, Perugia, Italy,
J Autism Dev Disord. 2014 Oct;44(10):2608-13. doi: 10.1007/s10803-014-2117-7.
The duplication of the Williams-Beuren syndrome (WBS) region (7q11.23) is a copy number variant associated with autism spectrum disorder (ASD). One of the most intriguing aspects is that the reciprocal microdeletion causes WBS, characterized by hypersociability, marked empathy, and a relative capacity in verbal short-term memory and language. Herein, we studied, by using functional morphological and volumetric magnetic resonance, a 17-year-old male patient who displays a de novo 7q11.23 duplication and ASD. The limbic system of the patient appeared hypo-functional, while the total brain volume was increased, thus contrasting, in an opposite and intriguing manner, with the global brain volume reduction reported in WBS. Even if these findings come from the analysis of a single patient and, therefore, have to be considered preliminary results, they encourage carrying on further functional and volumetric studies in patients with 7q11.23 duplication, to fully elucidate the role of this gene-dosage alteration on brain development and limbic system function.
威廉斯-贝伦综合征(WBS)区域(7q11.23)的重复是一种与自闭症谱系障碍(ASD)相关的拷贝数变异。最引人关注的方面之一是,与之相反的微缺失会导致WBS,其特征为过度社交、显著的同理心以及在言语短期记忆和语言方面的相对能力。在此,我们通过功能形态学和容积磁共振成像,研究了一名17岁男性患者,他表现出7q11.23的新发重复且患有ASD。该患者的边缘系统功能似乎减退,而全脑体积增加,这与WBS中报道的全脑体积减小形成了相反且有趣的对比。即使这些发现来自对一名患者的分析,因此必须被视为初步结果,但它们鼓励对7q11.23重复的患者进行进一步的功能和容积研究,以充分阐明这种基因剂量改变对大脑发育和边缘系统功能的作用。