Abstract

Although there is some consensus when it comes to establishing the lexicon as one of the strengths of language in people with Williams Syndrome (WS), little is known about its evolution throughout development and changes based on age. The objective of this study was to find out if there are differences in receptive vocabulary between childhood and adolescence and into adulthood. In this research, 19 people with WS between 6 and 20 years old, divided into two age ranges (6 - 11; 12 - 20) and matched in mental age, were evaluated through the Peabody Vocabulary Test. The results show significant differences between both groups in favor of the group with the oldest chronological age and a direct correlation between chronological age and receptive vocabulary development, regardless of mental age. These data support the natural evolution of the passive lexicon in people with WS.

Highlights

  • Williams Syndrome, hereinafter WS (Williams, Barratt-Boyes, & Lowe, 1961; Beuren, Apitz, & Harmjanz, 1962), is a neurodevelopmental disorder caused by a chromosome deletion on chromosome 7

  • There is some consensus when it comes to establishing the lexicon as one of the strengths of language in people with Williams Syndrome (WS), little is known about its evolution throughout development and changes based on age

  • The results show a higher level of receptive vocabulary in the group of adolescents and adults

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Summary

Introduction

Williams Syndrome, hereinafter WS (Williams, Barratt-Boyes, & Lowe, 1961; Beuren, Apitz, & Harmjanz, 1962), is a neurodevelopmental disorder caused by a chromosome deletion on chromosome 7. Some studies claim that Williams syndrome has an incidence of 1 case per 7500 approximately (Rossi & Giacheti, 2017; Strømme, Bjornstad, & Ramstad, 2002). On the other hand, say that the incidence is 1 in 20,000 (Garayzábal & Cuetos, 2008; Sotillo, 1999). WS is a multisystemic alteration that is reflected in the atypical neuroanatomic, physical-clinical, and neuropsychological phenotype. It manifests itself through cardiac and pulmonary alterations, prototypical facial features, and personality (Metcalfe, 1999; Rossi & Giacheti, 2017).

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