Abstract
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% [3-5]. 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.
Original language | English |
---|---|
Title of host publication | Moyamoya Disease Update |
Publisher | Springer Japan |
Pages | 114-117 |
Number of pages | 4 |
ISBN (Print) | 9784431997023 |
DOIs | |
Publication status | Published - 2010 Dec 1 |
ASJC Scopus subject areas
- Medicine(all)