Expressive and receptive vocabulary in children with Williams and Down syndromes.

BACKGROUND: Williams (WS) and Down syndromes (DS) are two genetic disorders that involve intellectual disability (ID) and have been extensively studied over the past decades because of the unique linguistic profiles they exhibit. Recent investigations seek to explore the fractionation of linguistic...

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Publicado en:Journal of Intellectual Disability Research Vol. 49; no. 5; pp. 353 - 365
Autores principales: Ypsilanti A, Grouios G, Alevriadou A, Tsapkini K
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell May2005
Acceso en línea:Ver este registro en EBSCOhost
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        atl: Expressive and receptive vocabulary in children with Williams and Down syndromes.
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          Ypsilanti A
          Grouios G
          Alevriadou A
          Tsapkini K
        affil: Department of Physical Education and Sport Sciences, Aristotele University of Thessaloniki, Thessaloniki, Greece
      sug:
        subj:
          Down Syndrome
          Vocabulary In Infancy and Childhood
          Williams Syndrome
          Adolescence
          Child
          Comparative Studies
          Data Analysis Software
          Descriptive Statistics
          Female
          Intelligence Tests
          Language Development
          Language Tests
          Male
          Matched Case Control
          One-Way Analysis of Variance
          Post Hoc Analysis
          Two-Tailed Test
          United Kingdom
          Human
          Adolescent: 13-18 years
          Child: 6-12 years
          Female
          Male
      ab: BACKGROUND: Williams (WS) and Down syndromes (DS) are two genetic disorders that involve intellectual disability (ID) and have been extensively studied over the past decades because of the unique linguistic profiles they exhibit. Recent investigations seek to explore the fractionation of linguistic components within the cognitive system using genetically based neurodevelopmental disorders such as WS and DS and to identify different profiles of linguistic function in these two groups of individuals. METHOD: The 'expressive vocabulary', 'receptive vocabulary', 'word opposites' and 'word definitions' subtests (Level 1) of the Test of Word Knowledge (TOWK) were used to assess lexical skills in six children with WS and five children with DS. RESULTS: Our findings indicate that the two syndromes exhibit substantial differences on linguistic tasks with individuals with WS performing at a higher level compared to those with DS and producing atypical responses in word definitions. The pattern of errors for each syndrome is qualitatively different suggesting that their underlying linguistic mechanisms are distinctive even though ID is similar. CONCLUSIONS: This study supports the differential outcome of two chromosomal disorders with similar ID. It also argues in favour of the large within group variability of the two syndromes that is not related to mental age but rather to different underlying mechanisms supporting language. These findings are discussed in the light of the current evidence concerning linguistic knowledge of neurodevelopmental and genetic disorders.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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