Effective dyslexia remediation specifically designed for older struggling readers (age 7+).

Strong Motion Deficits in Dyslexia Associated with DCDC2 Gene Alteration

G. M. Cicchini, C. Marino, S. Mascheretti, D. Perani, M. C. Morrone.
The Journal of Neuroscience, 27 May 2015, 35(21): 8059-8064; doi: 10.1523/JNEUROSCI.5077-14.2015

Abstract

Dyslexia is a specific impairment in reading that affects 1 in 10 people. Previous studies have failed to isolate a single cause of the disorder, but several candidate genes have been reported. We measured motion perception in two groups of dyslexics, with and without a deletion within the DCDC2 gene, a risk gene for dyslexia. We found impairment for motion particularly strong at high spatial frequencies in the population carrying the deletion. The data suggest that deficits in motion processing occur in a specific genotype, rather than the entire dyslexia population, contributing to the large variability in impairment of motion thresholds in dyslexia reported in the literature.

magnocellular-parvocellular system

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DYNAREAD: Grounded in Reality

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Dynaread has been developed in the trenches of actual remediation, with our feet firmly planted on the ground. Scientific research is essential (and we consistently use it), but we also understand the realities at home and in school. Not all homes have two parents, not all Dad's or Mom's are always home, there is oftentimes no money, schools lack staff or funding. We listen, we observe, we discuss, and we build the best solutions we can for older (ages 7+) struggling readers.

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