Oppenheim's or DYT1 dystonia is a primary dystonia typically presenting in a limb at an early age and usually becoming generalised within 5 years. Over the last decade research into this debilitating disorder has progressed considerably, enabling the identification of a genetic lesion (a 3bp deletion in the DYT1 gene) now widely accepted as the cause of a majority of cases. This case report presents the first molecularly diagnosed pedigree of an Australian family with DYT1 dystonia, which presented as writer's cramp in the 15-year-old proband and two of his cousins.
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http://dx.doi.org/10.1016/S0967-5868(03)00226-1 | DOI Listing |
Mov Disord Clin Pract
February 2025
Departments of Child Health, Neurology, and Cellular & Molecular Medicine, Program in Genetics, University of Arizona College of Medicine - Phoenix, Phoenix, Arizona, USA.
Nat Cell Biol
September 2024
Peter O'Donnell Jr. Brain Institute, UT Southwestern, Dallas, TX, USA.
As lifelong interphase cells, neurons face an array of unique challenges. A key challenge is regulating nuclear pore complex (NPC) biogenesis and localization, the mechanisms of which are largely unknown. Here we identify neuronal maturation as a period of strongly upregulated NPC biogenesis.
View Article and Find Full Text PDFbioRxiv
May 2024
Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
Neurobiol Dis
May 2024
Department of Neurology, University Hospital Würzburg, 97080, Germany. Electronic address:
DYT-TOR1A (DYT1) dystonia, characterized by reduced penetrance and suspected environmental triggers, is explored using a "second hit" DYT-TOR1A rat model. We aim to investigate the biological mechanisms driving the conversion into a dystonic phenotype, focusing on the striatum's role in dystonia pathophysiology. Sciatic nerve crush injury was induced in ∆ETorA rats, lacking spontaneous motor abnormalities, and wild-type (wt) rats.
View Article and Find Full Text PDFJ Neurosci
April 2024
Department of Biochemistry and Molecular Biology, Louisiana State University Health Sciences Center at Shreveport, Shreveport, Louisiana 71130-3932
DYT1 dystonia is a debilitating neurological movement disorder, and it represents the most frequent and severe form of hereditary primary dystonia. There is currently no cure for this disease due to its unclear pathogenesis. In our previous study utilizing patient-specific motor neurons (MNs), we identified distinct cellular deficits associated with the disease, including a deformed nucleus, disrupted neurodevelopment, and compromised nucleocytoplasmic transport (NCT) functions.
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