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Kover, Sara T.; McDuffie, Andrea; Abbeduto, Leonard; Brown, W. Ted – Journal of Speech, Language, and Hearing Research, 2012
Purpose: In this study, the authors examined the impact of sampling context on multiple aspects of expressive language in male participants with fragile X syndrome in comparison to male participants with Down syndrome or typical development. Method: Participants with fragile X syndrome (n = 27), ages 10-17 years, were matched groupwise on…
Descriptors: Expressive Language, Down Syndrome, Genetic Disorders, Mental Retardation
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
Finestack, Lizbeth H.; Abbeduto, Leonard – Journal of Speech, Language, and Hearing Research, 2010
Purpose: In this study, the authors examined the expressive language abilities of a subset of highly verbally expressive adolescents and young adults with Down syndrome (DS) and those with fragile X syndrome (FXS) for evidence of syndrome-related differences. FXS gender differences were also examined in an exploratory fashion. Method: The authors…
Descriptors: Adolescents, Expressive Language, Young Adults, Down Syndrome
Estigarribia, Bruno; Martin, Gary E.; Roberts, Joanne E. – Journal of Speech, Language, and Hearing Research, 2012
Purpose: To examine which cognitive, environmental, and speech-language variables predict expressive syntax in boys with fragile X syndrome (FXS), boys with Down syndrome (DS), and typically developing (TD) boys, and whether predictive relationships differed by group. Method: We obtained Index of Productive Syntax ( Scarborough, 1990) scores for…
Descriptors: Genetic Disorders, Mental Retardation, Congenital Impairments, Down Syndrome
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
Buckley, Sue – Down Syndrome Research and Practice, 2008
In recent years there has been much research interest in looking for behavioural phenotypes (or specific profiles of strengths and weaknesses) that are associated with specific conditions--particularly conditions with genetic origins such as Down syndrome. This kind of information may be very helpful in alerting parents and professionals to the…
Descriptors: Child Behavior, Down Syndrome, Genetic Disorders, Behavior Problems
Silverman, Wayne – Mental Retardation and Developmental Disabilities Research Reviews, 2007
Down syndrome is the most prevalent cause of intellectual impairment associated with a genetic anomaly, in this case, trisomy of chromosome 21. It affects both physical and cognitive development and produces a characteristic phenotype, although affected individuals vary considerably with respect to severity of specific impairments. Studies…
Descriptors: Down Syndrome, Auditory Perception, Short Term Memory, Expressive Language

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