| Literature DB >> 27448549 |
Antonio Costantini1, Erika Trevi2, Maria Immacolata Pala1, Roberto Fancellu3.
Abstract
Primary torsion dystonia is a movement disorder characterised by sustained or intermittent involuntary muscle contractions causing abnormal movements, postures or both. In this study, 3 brothers affected by inherited primary dystonia 16 (DYT16) began an oral therapy with high-dose thiamine from November to December 2015. After 3 months, an important improvement of the motor symptoms was observed. Our results support the hypothesis that pathogenesis of the symptoms might be related to a dysfunction in mitochondrial oxidative phosphorylation due to a focal impairment of thiamine-dependent processes. Our results support some authors' hypothesis that dystonia might have a mitochondrial aetiology. 2016 BMJ Publishing Group Ltd.Entities:
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Year: 2016 PMID: 27448549 PMCID: PMC4964157 DOI: 10.1136/bcr-2016-216721
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X