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Sterling, Audra – Journal of Speech, Language, and Hearing Research, 2018
Purpose: Some boys with autism spectrum disorder (ASD) and boys with fragile X syndrome and a codiagnosis of ASD (FXS+ASD) have impairments in expressive grammatical abilities. The current study compared grammatical performance in these 2 groups of school-age boys. Method: Thirty-seven boys similar on mean length of utterance participated in the…
Descriptors: Males, Autism, Pervasive Developmental Disorders, Genetic Disorders
Van Den Heuvel, E.; Manders, E.; Swillen, A.; Zink, I. – Journal of Intellectual Disability Research, 2016
Background: This study aimed to compare developmental courses of structural and pragmatic language skills in school-aged children with Williams syndrome (WS) and children with idiopathic intellectual disability (IID). Comparison of these language trajectories could highlight syndrome-specific developmental features. Method: Twelve monolingual…
Descriptors: Genetic Disorders, Language Skills, Children, Intellectual Disability
Thurman, Angela John; McDuffie, Andrea; Kover, Sara T.; Hagerman, Randi J.; Abbeduto, Leonard – Journal of Autism and Developmental Disorders, 2015
Although males with fragile X syndrome (FXS) are frequently described as demonstrating autism symptomatology, there is much debate regarding whether the behavioral symptoms representing the core domains of autism are the result of the same or different underlying neurological/psychological mechanisms. The present study used a cross-sectional…
Descriptors: Males, Genetic Disorders, Autism, Pervasive Developmental Disorders
Alfieri, P.; Menghini, D.; Marotta, L.; De Peppo, L.; Ravà, L.; Salvaguardia, F.; Varuzza, C.; Vicari, S. – Journal of Intellectual Disability Research, 2017
Background: Individuals with Williams syndrome (WS) show a disharmonic linguistic profile with a clear pattern of strengths and weaknesses. Despite their sociable nature, atypical socio-communicative abilities and deficits in communication and relationship with others have been found. Aim: The aim of the present study was to investigate whether…
Descriptors: Intellectual Disability, Genetic Disorders, Language Skills, Interpersonal Communication
Klusek, Jessica; Martin, Gary E.; Losh, Molly – American Journal on Intellectual and Developmental Disabilities, 2013
This study tested the hypothesis that pragmatic (i.e., social) language impairment is linked to arousal dysregulation in autism spectrum disorder (ASD) and fragile X syndrome (FXS). Forty boys with ASD, 39 with FXS, and 27 with typical development (TD), aged 4-15 years, participated. Boys with FXS were hyperaroused compared to boys with TD but did…
Descriptors: Physiology, Genetic Disorders, Pervasive Developmental Disorders, Autism
Skwerer, Daniela Plesa; Ammerman, Emily; Tager-Flusberg, Helen – Journal of Child Language, 2013
Research on language in individuals with Williams syndrome (WS) has been fueled by persistent theoretical controversies for two decades. These shifted from initial focus on dissociations between language and cognition functions, to examining the paradox of socio-communicative impairments despite high sociability and relatively proficient…
Descriptors: Genetic Disorders, Language Impairments, Communication Problems, Expressive Language
Finestack, Lizbeth H.; Sterling, Audra M.; Abbeduto, Leonard – Journal of Child Language, 2013
This study compared the receptive and expressive language profiles of verbally expressive children and adolescents with Down Syndrome (DS) and those with Fragile X syndrome (FXS) and examined the extent to which these profiles reliably differentiate the diagnostic groups. A total of twenty-four verbal participants with DS (mean age: 12 years),…
Descriptors: Expressive Language, Receptive Language, Verbal Communication, Children
Carney, Daniel P. J.; Brown, Janice H.; Henry, Lucy A. – Research in Developmental Disabilities: A Multidisciplinary Journal, 2013
Williams (WS) and Down (DS) syndromes are characterised by roughly opposing ability profiles. Relative verbal strengths and visuospatial difficulties have been reported in those with WS, while expressive language difficulties have been observed in individuals with DS. Few investigations into the executive function (EF) skills of these groups have…
Descriptors: Inhibition, Expressive Language, Executive Function, Down Syndrome
Martin, Gary E.; Losh, Molly; Estigarribia, Bruno; Sideris, John; Roberts, Joanne – International Journal of Language & Communication Disorders, 2013
Background: Fragile X syndrome (FXS) and Down syndrome (DS) are the two leading genetic causes of intellectual disability, and FXS is the most common known genetic condition associated with autism. Both FXS and DS are associated with significant language impairment, but little is known about expressive language across domains over time or the role…
Descriptors: Expressive Language, Vocabulary, Syntax, Pragmatics
Finestack, Lizbeth H.; Palmer, Meghan; Abbeduto, Leonard – American Journal of Speech-Language Pathology, 2012
Purpose: To gain a better understanding of language abilities, the expressive macrostructural narrative language abilities of verbally expressive adolescents and young adults with Down syndrome (DS) and those with fragile X syndrome (FXS) were examined. Method: The authors evaluated 24 adolescents and young adults with DS, 12 male adolescents and…
Descriptors: Down Syndrome, Young Adults, Adolescents, Genetic Disorders
Martinez-Castilla, Pastora; Stojanovik, Vesna; Setter, Jane; Sotillo, Maria – Applied Psycholinguistics, 2012
The aim of this study was to compare the prosodic profiles of English- and Spanish-speaking children with Williams syndrome (WS), examining cross-linguistic differences. Two groups of children with WS, English and Spanish, of similar chronological and nonverbal mental age, were compared on performance in expressive and receptive prosodic tasks…
Descriptors: Mental Age, Language Processing, Spanish Speaking, Contrastive Linguistics
Kover, S. T.; Abbeduto, L. – Journal of Intellectual Disability Research, 2010
Background: Approximately one-quarter of individuals with fragile X syndrome (FXS) meet diagnostic criteria for autism; however, it is unclear whether individuals with comorbid FXS and autism are simply more severely affected than their peers with only FXS or whether they have qualitatively different profiles of behavioural impairments. To address…
Descriptors: Genetic Disorders, Symptoms (Individual Disorders), Comparative Analysis, Males

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