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Autism Symptoms in Fragile X Syndrome.
Niu, Manman; Han, Ying; Dy, Angel Belle C; Du, Junbao; Jin, Hongfang; Qin, Jiong; Zhang, Jing; Li, Qinrui; Hagerman, Randi J.
Afiliación
  • Niu M; 1 Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Han Y; 1 Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Dy ABC; 2 MIND Institute, University of California, Davis, CA, USA.
  • Du J; 2 MIND Institute, University of California, Davis, CA, USA.
  • Jin H; 3 Ateneo de Manila University - School of Medicine and Public Health, Philippines.
  • Qin J; 1 Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Zhang J; 1 Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Li Q; 4 Department of Pediatrics, Peking University People's Hospital, Beijing, China.
  • Hagerman RJ; 1 Department of Pediatrics, Peking University First Hospital, Beijing, China.
J Child Neurol ; 32(10): 903-909, 2017 Sep.
Article en En | MEDLINE | ID: mdl-28617074
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno del Espectro Autista / Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: J Child Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno del Espectro Autista / Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: J Child Neurol Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos