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Understanding Comorbidity Between Specific Learning Disabilities.
Willcutt, Erik G; McGrath, Lauren M; Pennington, Bruce F; Keenan, Janice M; DeFries, John C; Olson, Richard K; Wadsworth, Sally J.
Afiliación
  • Willcutt EG; University of Colorado at Boulder.
  • McGrath LM; University of Denver.
  • Pennington BF; University of Denver.
  • Keenan JM; University of Denver.
  • DeFries JC; University of Colorado at Boulder.
  • Olson RK; University of Colorado at Boulder.
  • Wadsworth SJ; University of Colorado at Boulder.
New Dir Child Adolesc Dev ; 2019(165): 91-109, 2019 May.
Article en En | MEDLINE | ID: mdl-31070302
Current definitions of specific learning disability (SLD) identify a heterogeneous population that includes individuals with weaknesses in reading, math, or writing, and these academic difficulties often co-occur in many of the same individuals. The Colorado Learning Disabilities Research Center (CLDRC) is an interdisciplinary, multisite research program that uses converging levels of analysis to understand the genetic and environmental etiology, neuropsychology, and developmental outcomes of SLDs in reading (RD), math (MD), and writing (WD), along with the comorbidity between these SLDs and other developmental disorders. The latest results from the CLDRC twin study suggest that shared genetic influences contribute to the significant covariance between all aspects of reading (word reading, reading fluency, and reading comprehension) and math (calculations, math fluency, and word problems), and distinct genetic or environmental influences also contribute to weaknesses in each specific academic domain. RD and MD are associated with a range of negative outcomes on both concurrent measures and measures of functional outcomes completed 5 years after the twins were first assessed. Over the next several years the CLDRC will continue to expand on this work by administering a comprehensive test battery that includes measures of all dimensions of academic achievement that are described in current definitions of SLD and incorporating these measures in new neuroimaging and molecular genetic studies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dislexia / Discalculia Tipo de estudio: Etiology_studies Límite: Adolescent / Child / Humans Idioma: En Revista: New Dir Child Adolesc Dev Asunto de la revista: PEDIATRIA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dislexia / Discalculia Tipo de estudio: Etiology_studies Límite: Adolescent / Child / Humans Idioma: En Revista: New Dir Child Adolesc Dev Asunto de la revista: PEDIATRIA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos