Torniero Claudia, dalla Bernardina Bernardo, Novara Francesca, Vetro Annalisa, Ricca Ivana, Darra Francesca, Pramparo Tiziano, Guerrini Renzo, Zuffardi Orsetta
Servizio Neuropsichiatria Infantile, Policlinico GB Rossi, Studi di Verona, Verona, Italy.
Eur J Hum Genet. 2007 Jan;15(1):62-7. doi: 10.1038/sj.ejhg.5201730. Epub 2006 Oct 31.
We report on a new duplication case of 7q11.23, reciprocal of the Williams-Beuren (WB) deletion. The patient, a 13-year-old girl, was ascertained within an array-CGH screening of patients with epilepsy and neuronal migration defects. Similarly to the first reported patient, she showed serious difficulties in expressive language in the absence of severe mental retardation and marked dysmorphic features. Magnetic resonance imaging (MRI) of the brain revealed an abnormal development of the cerebral cortex in the left temporal lobe, which showed a simplified gyral pattern, and increased cortical thickness. This finding, which might explain poor language development, suggests that the WB critical region might harbour a dosage-sensitive gene controlling the molecular machinery of neuronal migration, with regional specificity and lateralization. It will be important to confirm our findings in newly diagnosed patients with dup(7)(q11.23). We expect to detect many more patients with the same duplication using widespread clinical implementation of high-resolution genome analysis.
我们报告了一例新的7q11.23重复病例,它是威廉姆斯-博伦综合征(WB)缺失的对应情况。该患者为一名13岁女孩,在对癫痫和神经元迁移缺陷患者进行的阵列比较基因组杂交(array-CGH)筛查中被确诊。与首例报道的患者相似,她在没有严重智力迟钝和明显畸形特征的情况下,表现出明显的语言表达困难。脑部磁共振成像(MRI)显示左颞叶大脑皮质发育异常,表现为脑回模式简化和皮质厚度增加。这一发现可能解释了语言发育不良的原因,表明WB关键区域可能含有一个剂量敏感基因,该基因控制着具有区域特异性和偏侧化的神经元迁移分子机制。在新诊断的dup(7)(q11.23)患者中证实我们的发现将很重要。我们预计,随着高分辨率基因组分析在临床中的广泛应用,会发现更多患有相同重复的患者。