Literature DB >> 28617074

Autism Symptoms in Fragile X Syndrome.

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


  24 in total

Review 1.  Response to name and its value for the early detection of developmental disorders: Insights from autism spectrum disorder, Rett syndrome, and fragile X syndrome. A perspectives paper.

Authors:  Dajie Zhang; Laura Roche; Katrin D Bartl-Pokorny; Magdalena Krieber; Laurie McLay; Sven Bölte; Luise Poustka; Jeff Sigafoos; Markus Gugatschka; Christa Einspieler; Peter B Marschik
Journal:  Res Dev Disabil       Date:  2018-04-12

2.  The Genetic Control of Stoichiometry Underlying Autism.

Authors:  Robert B Darnell
Journal:  Annu Rev Neurosci       Date:  2020-07-08       Impact factor: 12.449

3.  Retinoic Acid Supplementation Rescues the Social Deficits in Fmr1 Knockout Mice.

Authors:  Liqin Yang; Zhixiong Xia; Jianhua Feng; Menghuan Zhang; Pu Miao; Yingjie Nie; Xiangyan Zhang; Zijian Hao; Ronggui Hu
Journal:  Front Genet       Date:  2022-06-17       Impact factor: 4.772

4.  How Is CYP17A1 Activity Altered in Autism? A Pilot Study to Identify Potential Pharmacological Targets.

Authors:  Benedikt Andreas Gasser; Johann Kurz; Bernhard Dick; Markus Georg Mohaupt
Journal:  Life (Basel)       Date:  2022-06-10

5.  ASD Comorbidity in Fragile X Syndrome: Symptom Profile and Predictors of Symptom Severity in Adolescent and Young Adult Males.

Authors:  Leonard Abbeduto; Angela John Thurman; Andrea McDuffie; Jessica Klusek; Robyn Tempero Feigles; W Ted Brown; Danielle J Harvey; Tatyana Adayev; Giuseppe LaFauci; Carl Dobkins; Jane E Roberts
Journal:  J Autism Dev Disord       Date:  2019-03

6.  A single early-life seizure results in long-term behavioral changes in the adult Fmr1 knockout mouse.

Authors:  Samantha L Hodges; Conner D Reynolds; Suzanne O Nolan; Jessica L Huebschman; James T Okoh; Matthew S Binder; Joaquin N Lugo
Journal:  Epilepsy Res       Date:  2019-08-29       Impact factor: 3.045

Review 7.  Mechanisms underlying auditory processing deficits in Fragile X syndrome.

Authors:  Elizabeth A McCullagh; Sarah E Rotschafer; Benjamin D Auerbach; Achim Klug; Leonard K Kaczmarek; Karina S Cramer; Randy J Kulesza; Khaleel A Razak; Jonathan W Lovelace; Yong Lu; Ursula Koch; Yuan Wang
Journal:  FASEB J       Date:  2020-02-10       Impact factor: 5.191

8.  Brief Report: Linguistic Mazes and Perseverations in School-Age Boys with Fragile X Syndrome and Autism Spectrum Disorder and Relationships with Maternal Maze Use.

Authors:  Nell Maltman; Laura Friedman; Emily Lorang; Audra Sterling
Journal:  J Autism Dev Disord       Date:  2021-03-25

9.  The broader autism phenotype constellations-disability matrix paradigm: Theoretical model for autism and the broader autism phenotype.

Authors:  T A Meridian McDonald
Journal:  Med Hypotheses       Date:  2020-12-18       Impact factor: 1.538

10.  Loss of Tsc1 in cerebellar Purkinje cells induces transcriptional and translation changes in FMRP target transcripts.

Authors:  Jasbir Singh Dalal; Kellen Diamond Winden; Catherine Lourdes Salussolia; Maria Sundberg; Achint Singh; Truc Thanh Pham; Pingzhu Zhou; William T Pu; Meghan T Miller; Mustafa Sahin
Journal:  Elife       Date:  2021-07-14       Impact factor: 8.140

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