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Updated: Jul 25, 2026

Co-analysis of Brain Structure and Function using fMRI and Diffusion-weighted Imaging
Published on: November 8, 2012
White matter tract involvement in anarchic hand syndrome following stroke: Diffusion tensor imaging study
Jihee Park1, Woo-Suk Tae2, Sekwang Lee1
1Department of Physical Medicine and Rehabilitation, Anam Hospital, Korea University College of Medicine, Seoul, South Korea.
None:
Anarchic Hand Syndrome (AHS) is a rare neurological disorder characterized by involuntary, purposeful hand movements. AHS can also result from damage to the corpus callosum (CC), intra-hemispheric tracts, or descending tracts, but its precise causes remain unclear. This study aimed to identify the white matter tracts associated with AHS development using the automated reconstruction of 42 tracts from diffusion tensor imaging (DTI). We included three female AHS patients with anterior cerebral arterial (ACA) infarctions. Additionally, we enrolled 20 age-matched control subjects and six patients with ACA infarctions but without AHS symptoms (N-AHS group) for comparison. DTI was conducted in AHS, N-AHS, and control groups. Fractional anisotropy (FA) and volume values were extracted from the DTI datasets of participants using TRActs Constrained by UnderLying Anatomy (TRACULA) technique. The AHS group showed lower FA values of the CC body (parietal and temporal section), right arcuate fasciculus (AF), corticospinal tract, extreme capsule, inferior longitudinal fasciculus (ILF), and superior longitudinal fasciculus than the control group. However, these tracts exhibited no significant difference between N-AHS and control groups. Similarly, the volume value in the genu of CC in the AHS group was lower than controls, but not in other tracts. Our results suggests that the extensive CC lesion, especially in the posterior parietal and temporal section of CC body, and damage to intra-hemispheric tracts (AF and ILF), is associated with the development of AHS. These results involved in AHS and underscore the significance of considering a more complex network disruption, involving various white matter tracts beyond CC for understanding this syndrome.
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