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Acta Neurologica Belgica

, Volume 117, Issue 4, pp 955–956 | Cite as

Dopa-responsive dystonia presenting with predominant hemifacial dystonia

  • Min Seung Kim
  • Jung Han YoonEmail author
Letter to the Editor
  • 171 Downloads

Dear Editor,

Dopa-responsive dystonia (DRD) encompasses a group of clinically and genetically heterogeneous disorders that respond markedly well to l-DOPA [1]. Most cases begin with dystonia in a lower extremity, which progresses to segmental or generalized dystonia [2]. However, DRD is clinically and genetically heterogenous disorders, which often leads to misdiagnosis, which delays treatment. Here, we report a young woman with DRD presenting with subacute-onset hemifacial dystonia.

A 23-year-old woman was admitted to our hospital with a several-month history of right hemifacial dystonia. She had been born by a normal delivery and her development had been normal. There was no family history of movement disorders. Initially, facial dystonia began in the morning and lasted for short periods (several minutes). No diurnal fluctuations were observed. Over several months, the duration of the dystonia lengthened progressively and eventually continued throughout the day. The patient’s...

Keywords

Dystonia Pramipexole Entacapone Carbidopa Focal Dystonia 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Compliance with ethical standards

Conflict of interest

The authors have no conflicts of interest or financial support to report.

Ethical approval

The institutional review board at Ajou Hospital approved this case report.

Informed consent

The patients have consented to the submission of the case report to the journal.

Supplementary material

Supplementary material 1 (WMV 10,032 kb)

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Copyright information

© Belgian Neurological Society 2017

Authors and Affiliations

  1. 1.Department of NeurologyAjou University School of MedicineSuwonSouth Korea

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