Childhood-Onset Myoclonus-Dystonia Due to KCTD17 Mutation: A Case Report and Review of Diagnostic Challenges
By: Yun Lin, Yu Aoh and Ming-Kuei Lu
Authors
Division of Parkinson’s Disease and Movement Disorders, Department of Neurology, China Medical University Hospital, Taichung
Division of Parkinson’s Disease and Movement Disorders, Department of Neurology, China Medical University Hospital, Taichung; Graduate Institute of Biomedical Sciences, College of Medicine, China Medical University, Taichung
Division of Parkinson’s Disease and Movement Disorders, Department of Neurology, China Medical University Hospital, Taichung; Neuroscience and Brain Disease Center, China Medical University, Taichung; School of Medicine, College of Medicine, China Medical University, Taichung; Division of Neurology, Taichung Municipal Geriatric Rehabilitation General Hospital, China Medical University, Taichung
DOI: https://doi.org/10.5334/tohm.1170 | Journal eISSN: 2160-8288
Language: English
Page range: 24 - 24
Submitted on: Jan 20, 2026
Accepted on: Mar 31, 2026
Published on: Apr 9, 2026
Published by: Ubiquity Press
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
Keywords:
© 2026 Yun Lin, Yu Aoh, Ming-Kuei Lu, published by Ubiquity Press
This work is licensed under the Creative Commons Attribution 4.0 License.