Bilder Deborah A, Bakian Amanda V, Stevenson David A, Carbone Paul S, Cunniff Christopher, Goodman Alyson B, McMahon William M, Fisher Nicole P, Viskochil David
Utah Autism Research Program, Department of Psychiatry, University of Utah, 650 Komas Drive, Suite 206, Salt Lake City, UT, 84108, USA.
Division of Medical Genetics, University of Utah, Salt Lake City, UT, USA.
J Autism Dev Disord. 2016 Oct;46(10):3369-76. doi: 10.1007/s10803-016-2877-3.
Neurofibromatosis type 1 (NF1) is an inherited neurocutaneous disorder associated with neurodevelopmental disorders including autism spectrum disorder (ASD). The frequency of ASD/NF1 co-occurrence has been subject to debate since the 1980s. This relationship was investigated in a large population-based sample of 8-year-old children identified with ASD (N = 12,271) by the Centers for Disease Control and Prevention's Autism and Developmental Disabilities Monitoring (ADDM) Network. Twenty-two (1-in-558) children with ASD had diagnosed NF1, exceeding NF1 general population estimates by four to five fold. Children with ASD/NF1 versus ASD without NF1 were significantly less likely to receive a community-based ASD diagnosis (p = 0.04) and understand non-verbal communication (p = 0.001). These findings underscore the importance of including social-communication ability among relevant developmental concerns in children with NF1.
1型神经纤维瘤病(NF1)是一种遗传性神经皮肤疾病,与包括自闭症谱系障碍(ASD)在内的神经发育障碍有关。自20世纪80年代以来,ASD/NF1共现的频率一直存在争议。美国疾病控制与预防中心的自闭症及发育障碍监测(ADDM)网络,在一个以大量8岁自闭症儿童为基础的样本(N = 12271)中对这种关系进行了调查。22名(1/558)患有ASD的儿童被诊断出患有NF1,这一比例超过了一般人群中NF1的估计值四到五倍。与没有NF1的ASD儿童相比,患有ASD/NF1的儿童获得基于社区的ASD诊断(p = 0.04)和理解非语言交流(p = 0.001)的可能性显著降低。这些发现强调了在NF1儿童相关发育问题中纳入社会沟通能力的重要性。