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Late-onset axial jerky dystonia due to the DYT1 deletion

Lookup NU author(s): Professor Patrick Chinnery, Professor Sir John Burn

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Abstract

We describe a 71-year-old woman who presented to the neurology department late in life with a jerky axial dystonia due to the DYT1 GAG deletion. She recalled that her symptoms began 62 years prior to study and remained unchanged for 40 years, illustrating the broad phenotype of DYT1 idiopathic torsion dystonia. © 2001 Movement Disorder Society.


Publication metadata

Author(s): Chinnery PF, Reading PJ, McCarthy EL, Curtis A, Burn J

Publication type: Article

Publication status: Published

Journal: Movement Disorders

Year: 2002

Volume: 17

Issue: 1

Pages: 196-198

Print publication date: 01/01/2002

ISSN (print): 0885-3185

ISSN (electronic): 1531-8257

Publisher: Wiley-Blackwell Publishing

URL: http://dx.doi.org/10.1002/mds.10021

DOI: 10.1002/mds.10021

PubMed id: 11835464


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