TY - JOUR A1 - Neuhoff, Nina A1 - Bruder, Jennifer A1 - Bartling, Jürgen A1 - Warnke, Andreas A1 - Remschmidt, Helmut A1 - Müller-Myhsok, Bertram A1 - Schulte-Körne, Gerd T1 - Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia JF - PLoS One N2 - Dyslexia affects 5-10% of school-aged children and is therefore one of the most common learning disorders. Research on auditory event related potentials (AERP), particularly the mismatch negativity (MMN) component, has revealed anomalies in individuals with dyslexia to speech stimuli. Furthermore, candidate genes for this disorder were found through molecular genetic studies. A current challenge for dyslexia research is to understand the interaction between molecular genetics and brain function, and to promote the identification of relevant endophenotypes for dyslexia. The present study examines MMN, a neurophysiological correlate of speech perception, and its potential as an endophenotype for dyslexia in three groups of children. The first group of children was clinically diagnosed with dyslexia, whereas the second group of children was comprised of their siblings who had average reading and spelling skills and were therefore "unaffected'' despite having a genetic risk for dyslexia. The third group consisted of control children who were not related to the other groups and were also unaffected. In total, 225 children were included in the study. All children showed clear MMN activity to/da/-/ba/ contrasts that could be separated into three distinct MMN components. Whilst the first two MMN components did not differentiate the groups, the late MMN component (300-700 ms) revealed significant group differences. The mean area of the late MMN was attenuated in both the dyslexic children and their unaffected siblings in comparison to the control children. This finding is indicative of analogous alterations of neurophysiological processes in children with dyslexia and those with a genetic risk for dyslexia, without a manifestation of the disorder. The present results therefore further suggest that the late MMN might be a potential endophenotype for dyslexia. KW - processing deficits KW - children KW - event-related potentials KW - mismatch negativity mmn KW - developmental dyslexia KW - reading disability KW - auditory discrimination KW - susceptibility gene KW - speech perception KW - novelty detection Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-133686 VL - 7 IS - 5 ER - TY - JOUR A1 - Huestegge, Lynn A1 - Rohrßen, Julia A1 - van Ermingen-Marbach, Muna A1 - Pape-Neumann, Julia A1 - Heim, Stefan T1 - Devil in the details ? Developmental dyslexia and visual long-term memory for details JF - Frontiers in Psychology N2 - Cognitive theories on causes of developmental dyslexia can be divided into language-specific and general accounts. While the former assume that words are special in that associated processing problems are rooted in language-related cognition (e.g., phonology) deficits, the latter propose that dyslexia is rather rooted in a general impairment of cognitive (e.g., visual and/or auditory) processing streams. In the present study, we examined to what extent dyslexia (typically characterized by poor orthographic representations) may be associated with a general deficit in visual long-term memory (LTM) for details. We compared object- and detail-related visual LTM performance (and phonological skills) between dyslexic primary school children and IQ-, age-, and gender-matched controls. The results revealed that while the overall amount of LTM errors was comparable between groups, dyslexic children exhibited a greater portion of detail-related errors. The results suggest that not only phonological, but also general visual resolution deficits in LTM may play an important role in developmental dyslexia. KW - anguage and word processing KW - picture processing KW - memory errors KW - orthographic representations KW - visual resolution deficit KW - phonology and reading KW - word form area KW - reading disability KW - spatial attention KW - ventral stream Y1 - 2014 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-115887 SN - 1664-1078 VL - 5 IS - 686 ER -