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Part of the book series: Principles of Pediatric Neurosurgery ((PRINCPEDIATR))

Abstract

At the fourteenth meeting of the Japanese Neurosurgical Society in 1955, Shimizu and Takeuchi reported a new disease entity designated as dysplasia of both internal carotid arteries1. This appears to be the first report of what we now refer to as moyamoya disease2. A succession of reports by a number of Japanese neurosurgeons3–6 of a similar disease followed, and the pathology of the disease was found to be characterized by the bilateral formation of abnormal netlike vessels at the base of the brain, associated with bilateral stenosis and/or occlusion of the arteries composing the circle of Willis.

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Sato, K., Shimoji, T. (1992). Moyamoya Disease. In: Raimondi, A.J., Choux, M., Di Rocco, C. (eds) Cerebrovascular Diseases in Children. Principles of Pediatric Neurosurgery. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-2800-4_17

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