Brief Report: The Prevalence of Neurofibromatosis Type 1 among Children with Autism Spectrum Disorder Identified by the Autism and Developmental Disabilities Monitoring Network

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-ba...

Full description

Saved in:
Bibliographic Details
Published inJournal of autism and developmental disorders Vol. 46; no. 10; pp. 3369 - 3376
Main Authors 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
Format Journal Article
LanguageEnglish
Published New York Springer US 01.10.2016
Springer
Springer Nature B.V
Subjects
Online AccessGet full text
ISSN0162-3257
1573-3432
1573-3432
DOI10.1007/s10803-016-2877-3

Cover

More Information
Summary: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.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:0162-3257
1573-3432
1573-3432
DOI:10.1007/s10803-016-2877-3