Cortical and Striatal Functional Connectivity in Juvenile-Onset Huntington’s Disease
Background: Huntington’s disease (HD) is a neurodegenerative disorder caused by a CAG repeat expansion in the HTT gene, with a rare juvenile-onset form (JoHD) marked by early, rigid motor symptoms. This study examined cortical and subcortical resting-state connectivity in JoHD, hypothesizing preserv...
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Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2025-06-01
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Series: | Brain Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/2076-3425/15/6/663 |
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