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Corpus callosum morphology in children who stutter
Ai Leen Choo1, Soo-Eun Chang, Hatun Zengin-Bolatkale
1Department of Speech and Hearing Science, University of Illinois at Urbana-Champaign, 901 S. Sixth Street, Champaign, IL 61820, USA. choo1@illinois.edu
Structural brain differences in children who stutter are not evident in the corpus callosum. Research found no differences in corpus callosum size or white matter volume in children who stutter compared to typically developing peers.
Area of Science:
- Neuroanatomy
- Developmental neuroscience
- Speech and language disorders
Background:
- Previous studies indicate functional and neuroanatomical differences in adults who stutter.
- Developmental data suggest potential structural brain differences in school-aged children who stutter.
- The role of the corpus callosum in stuttering is not fully understood.
Purpose of the Study:
- To investigate if aberrant corpus callosum morphology is implicated in persistent childhood stuttering.
- To compare the corpus callosum in children with persistent stuttering, recovered stuttering, and typically developing children.
- To examine developmental differences in corpus callosum anatomy related to stuttering.
Main Methods:
- Compared the corpus callosum midsagittal area and subsection areas in children aged 9-12.
- Utilized Medical Image Processing, Analysis, and Visualization (MIPAV) for measurements.
- Employed voxel-based morphometry (VBM) to compare white matter volume.
Main Results:
- No significant differences were detected in total corpus callosum area or white matter volume.
- No differences were found in specific corpus callosum subsections (rostrum, anterior midbody, posterior midbody, splenium).
- Findings align with dichotic listening studies showing a typical right ear advantage in children who stutter.
Conclusions:
- Aberrant callosal morphology is not implicated in childhood stuttering.
- Observed neural reorganization in adults who stutter may be a long-term adaptation.
- Childhood stuttering does not appear to stem from structural midline brain differences.
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