Involuntary Movement

  • Shigeru Nogawa
  • Norihiro Suzuki


Moyamoya disease is an idiopathic cerebrovascular disease characterized by progressive steno-occlusion of the arteries of the circle of Willis, accompanied by collateral vessel formation in the basal ganglia [1, 2]. Involuntary movements are relatively rare symptoms of this condition, and their frequency is estimated to range from 3 to 6% [3, 4, 5]. However, the incidence could be higher, if limb shaking, a specific type of transient ischemic attack (TIA), is also included. In this chapter, we focus on moyamoya disease-induced involuntary movements, and the patient characteristics, symptoms, underlying mechanisms, and treatment of this condition are discussed.


Basal Ganglion Internal Carotid Artery Transient Ischemic Attack Involuntary Movement Moyamoya Disease 
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Copyright information

© Springer 2010

Authors and Affiliations

  1. 1.Department of NeurologyTokyo Dental College Ichikawa General HospitalIchikawaJapan
  2. 2.Department of NeurologyKeio University School of MedicineShinjuku-kuJapan

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