Your browser doesn't support javascript.
loading
Characterizing the Richness of Maternal Input for Word Learning in Neurogenetic Disorders.
Mattie, Laura J; Hadley, Pamela A.
Afiliación
  • Mattie LJ; Department of Speech and Hearing Science, University of Illinois at Urbana-Champaign, Champaign, Illinois.
  • Hadley PA; Department of Speech and Hearing Science, University of Illinois at Urbana-Champaign, Champaign, Illinois.
Semin Speech Lang ; 42(4): 301-317, 2021 08.
Article en En | MEDLINE | ID: mdl-34311482
ABSTRACT
Promoting language abilities, including early word learning, in children with neurogenetic disorders with associated language disorders, such as Down syndrome (DS) and fragile X syndrome (FXS), is a main concern for caregivers and clinicians. For typically developing children, the quality and quantity of maternal language input and maternal gesture use contributes to child word learning, and a similar relation is likely present in DS and FXS. However, few studies have examined the combined effect of maternal language input and maternal gesture use on child word learning. We present a multidimensional approach for coding word-referent transparency in naturally occurring input to children with neurogenetic disorders. We conceptualize high-quality input from a multidimensional perspective, considering features from linguistic, interactive, and conceptual dimensions simultaneously. Using case examples, we highlight how infrequent the moments of word-referent transparency are for three toddlers with DS during play with their mothers. We discuss the implications of this multidimensional framework for children with DS and FXS, including the clinical application of our approach to promote early word learning for these children.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Down / Síndrome del Cromosoma X Frágil Límite: Humans Idioma: En Revista: Semin Speech Lang Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Down / Síndrome del Cromosoma X Frágil Límite: Humans Idioma: En Revista: Semin Speech Lang Año: 2021 Tipo del documento: Article