| Literature DB >> 27465244 |
Deborah A Bilder1, Amanda V Bakian2, David A Stevenson3,4, Paul S Carbone5, Christopher Cunniff6,7, Alyson B Goodman8, William M McMahon9, Nicole P Fisher9, David Viskochil3.
Abstract
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.Entities:
Keywords: Autism; Children; Developmental disabilities; Neurofibromatosis; Non-verbal communications
Mesh:
Year: 2016 PMID: 27465244 PMCID: PMC5494711 DOI: 10.1007/s10803-016-2877-3
Source DB: PubMed Journal: J Autism Dev Disord ISSN: 0162-3257