ArticleAnnals of African medicine
Dystonia, myoclonus, and encephalopathy in a single patient: A rare association of moyamoya.
Article in Annals of African medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed, 0 citations in OpenAlex.
- Dystonia as the Initial Manifestation of Moyamoya Disease: A Case Report and Literature Review.Case reports in neurologyArticle
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4 authors at 4 institutions in 1 country.
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Abstract
Moyamoya disease (MMD) is a rare neurovascular disorder which pathologically, is a chronic cerebrovasculopathy. It is characterized by stenosis of the internal carotid artery (ICA) and the main branches within the circle of Willis with consecutive development of collateral vessels. There are a few cases in the literature which have described movement disorders as a manifestation of MMD; however these have been uncommonly reported in cases of moyamoya syndrome (MMS). We present a 10-year-old boy with dystonia, myoclonus and encephalopathy like features. These features in association with moyamoya, are rarely described.
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