| Literature DB >> 28617074 |
Manman Niu1, Ying Han1,2, Angel Belle C Dy2,3, Junbao Du1, Hongfang Jin1, Jiong Qin4, Jing Zhang1, Qinrui Li1, Randi J Hagerman2,5.
Abstract
Fragile X syndrome (FXS) is recognized as the most common genetic cause of intellectual disability and autism spectrum disorder (ASD). Although symptoms of ASD are frequently observed in patients with FXS, researchers have not yet clearly determined whether the symptoms in patients with FXS differ from the symptoms in patients without ASD or nonsyndromic ASD. Behavioral similarities and differences between FXS and ASD are important to improve our understanding of the causes and correlations of ASD with FXS. Based on the evidence presented in this review, individuals with FXS and comorbid ASD have more severe behavioral problems than individuals with FXS alone. However, patients with FXS and comorbid ASD exhibit less severe impairments in the social and communication symptoms than patients with nonsyndromic ASD. Individuals with FXS also present with anxiety and seizures in addition to comorbid ASD symptoms, and differences in these conditions are noted in patients with FXS and ASD. This review also discusses the role of fragile X mental retardation 1 protein (FMRP) in FXS and ASD phenotypes.Entities:
Keywords: anxiety; autism spectrum disorder; fragile X mental retardation 1 protein; fragile X syndrome; seizures
Mesh:
Year: 2017 PMID: 28617074 DOI: 10.1177/0883073817712875
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987