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The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on.
Guidi, Luiz G; Velayos-Baeza, Antonio; Martinez-Garay, Isabel; Monaco, Anthony P; Paracchini, Silvia; Bishop, Dorothy V M; Molnár, Zoltán.
Afiliación
  • Guidi LG; Department of Physiology, Anatomy, and Genetics, University of Oxford, Oxford, UK.
  • Velayos-Baeza A; Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Martinez-Garay I; Department of Physiology, Anatomy, and Genetics, University of Oxford, Oxford, UK.
  • Monaco AP; Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Paracchini S; Department of Physiology, Anatomy, and Genetics, University of Oxford, Oxford, UK.
  • Bishop DVM; Division of Neuroscience, School of Biosciences, Cardiff University, Cardiff, UK.
  • Molnár Z; Office of the President, Tufts University, Medford, Massachusetts.
Eur J Neurosci ; 48(10): 3212-3233, 2018 11.
Article en En | MEDLINE | ID: mdl-30218584
ABSTRACT
The capacity for language is one of the key features underlying the complexity of human cognition and its evolution. However, little is known about the neurobiological mechanisms that mediate normal or impaired linguistic ability. For developmental dyslexia, early postmortem studies conducted in the 1980s linked the disorder to subtle defects in the migration of neurons in the developing neocortex. These early studies were reinforced by human genetic analyses that identified dyslexia susceptibility genes and subsequent evidence of their involvement in neuronal migration. In this review, we examine recent experimental evidence that does not support the link between dyslexia and neuronal migration. We critically evaluate gene function studies conducted in rodent models and draw attention to the lack of robust evidence from histopathological and imaging studies in humans. Our review suggests that the neuronal migration hypothesis of dyslexia should be reconsidered, and the neurobiological basis of dyslexia should be approached with a fresh start.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Movimiento Celular / Neocórtex / Predisposición Genética a la Enfermedad / Modelos Animales de Enfermedad / Dislexia / Neuronas Límite: Animals / Humans Idioma: En Revista: Eur J Neurosci Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: FR / FRANCE / FRANCIA / FRANÇA

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Movimiento Celular / Neocórtex / Predisposición Genética a la Enfermedad / Modelos Animales de Enfermedad / Dislexia / Neuronas Límite: Animals / Humans Idioma: En Revista: Eur J Neurosci Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: FR / FRANCE / FRANCIA / FRANÇA