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DOI 10.1016/j.clinph.2012.12.044

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2013

Neural evidence of the allophonic mode of speech perception in adults with dyslexia.

Noordenbos Mark W, Segers Eliane, Serniclaes Willy, Verhoeven Ludo

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Аннотация

OBJECTIVE

A growing body of evidence suggests that individuals with dyslexia perceive speech using allophonic rather than phonemic units and are thus sensitive to phonetic variations that are actually irrelevant in the ambient language. This study investigated speech perception difficulties in adults with dyslexia using behavioural and neural measurements with stimuli along a place-of-articulation continuum with well-defined allophonic boundaries. Adults without dyslexia served as control participants.

METHODS

Categorical perception of a /bə - də/ place-of-articulation continuum was evaluated using both identification and discrimination tasks. In addition to these behavioural measures, mismatch negativity (MMN) was recorded for stimuli that came from either similar or different phoneme categories.

RESULTS

The adults with dyslexia exhibited less consistent labelling than controls, but no heightened sensitivity to allophonic contrasts was observed at the behavioural level. Neural measurements revealed that stimuli from different phoneme categories elicited MMNs in both the adults with dyslexia and controls, whereas stimuli from the same category elicited an MMN in the adults with dyslexia only.

CONCLUSION

The finding that adults with dyslexia have heightened sensitivity to allophonic contrasts in the form of neural activation supports the allophonic explanation of dyslexia.

SIGNIFICANCE: Sensitivity to allophonic contrasts may be a valuable marker for dyslexia.

Для цитирования: Noordenbos Mark W, Segers Eliane, Serniclaes Willy, Verhoeven Ludo. Neural evidence of the allophonic mode of speech perception in adults with dyslexia.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2013. DOI: 10.1016/j.clinph.2012.12.044.

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