Alfieri Paolo, Piccini Giorgia, Caciolo Cristina, Perrino Francesca, Gambardella Maria Luigia, Mallardi Maria, Cesarini Laura, Leoni Chiara, Leone Daniela, Fossati Chiara, Selicorni Angelo, Digilio Maria Cristina, Tartaglia Marco, Mercuri Eugenio, Zampino Giuseppe, Vicari Stefano
Dipartimento di Neuroscienze, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Am J Med Genet A. 2014 Apr;164A(4):934-42. doi: 10.1002/ajmg.a.36374. Epub 2014 Jan 23.
Here, we describe neurobehavioral features in patients with RASopathies (i.e., Noonan syndrome, LEOPARD syndrome, Costello syndrome, and cardiofaciocutaneous syndrome), developmental disorders caused by mutations in genes coding transducers participating in the RAS-MAPK signaling cascade. Parents of 70 individuals with a RASopathy were asked to fill out the following questionnaires: Child Behavior Checklist (CBCL), Social Communication Questionnaire version lifetime (SCQ-L), and Modified Checklist for Autism in toddlers (M-CHAT). Data analysis indicated high rates of internalizing (37%) and externalizing problems (31%) on CBCL. Scores over the cut-off were documented in 64% of patients with cardiofaciocutaneous syndrome, 44% with Costello syndrome, and 12% with Noonan syndrome on SCQ-L/M-CHAT. Our findings indicate that mutations promoting dysregulation of the RAS-MAPK cascade mark an increased psychopathological risk and highlight that autistic-like behavior could be underdiagnosed in patients with RASopathies.
在此,我们描述了患有RAS病(即努南综合征、豹皮综合征、科斯特洛综合征和心脏颜面皮肤综合征)患者的神经行为特征,这些发育障碍是由参与RAS-MAPK信号级联反应的转导子基因突变引起的。我们邀请了70名患有RAS病患者的家长填写以下问卷:儿童行为检查表(CBCL)、终身版社会沟通问卷(SCQ-L)和幼儿自闭症改良检查表(M-CHAT)。数据分析表明,CBCL上内化问题(37%)和外化问题(31%)的发生率很高。在SCQ-L/M-CHAT上,64%的心脏颜面皮肤综合征患者、44%的科斯特洛综合征患者和12%的努南综合征患者的得分超过了临界值。我们的研究结果表明,促进RAS-MAPK级联反应失调的突变标志着心理病理风险增加,并强调RAS病患者的自闭症样行为可能未得到充分诊断。