Paroxysmal kinesigenic dyskinesia: a diagnostic challenge

BMJ Case Rep. 2021 Feb 5;14(2):e235112. doi: 10.1136/bcr-2020-235112.

Abstract

A 10-year-old girl presented with a month long history of episodic limb movements. She had a normal neurological examination and after thorough investigation, she was thought to have possible tics. Anxiety was reported as being a trigger. Unusually, these 'tics' were not directly witnessed during hospital visits. Eighteen months after the initial presentation, the clinician observed dystonic posturing after the child stood up from having been seated during a consultation. Paroxysmal kinesigenic dyskinesia (PKD) was then suspected and confirmed on genetic testing. She was successfully treated with carbamazepine. In hindsight, it became apparent that her anxiety was related to a fear of uncontrolled movements, rather than it being a trigger. The abnormal involuntary movements in PKD are precipitated by sudden voluntary movement. Lack of recognition of this typical feature, normal examination and/or features such as coexisting anxiety can lead to misdiagnosis or delayed diagnosis of this easily treatable condition.

Keywords: movement disorders (other than Parkinsons); paediatrics.

Publication types

  • Case Reports
  • Video-Audio Media

MeSH terms

  • Anticonvulsants / therapeutic use
  • Carbamazepine / therapeutic use
  • Child
  • Diagnosis, Differential
  • Dystonia / diagnosis*
  • Dystonia / drug therapy
  • Dystonia / genetics
  • Dystonia / psychology
  • Female
  • Humans

Substances

  • Anticonvulsants
  • Carbamazepine

Supplementary concepts

  • Familial paroxysmal dystonia