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Moyamoya Disease in a 4‐Year‐Old Male Child: A Case Report From Nepal
1 Introduction Moyamoya disease (MMD) is a rare, progressive cerebrovascular disorder caused by bilateral stenosis or occlusion of the terminal portion of the internal carotid arteries (ICAs) and/or the proximal portions of the anterior cerebral arteries (ACAs) and middle cerebral arteries (MCAs) [1]. MMD means “puff of smoke” in Japanese and is used to describe the abnormal tangled vascular network compensating for the blockage [2].
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