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Dystonia, myoclonus, and encephalopathy in a single patient: A rare association of moyamoya
- Source :
- Annals of African Medicine
- Publication Year :
- 2016
- Publisher :
- Medknow Publications & Media Pvt Ltd, 2016.
-
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.
- Subjects :
- medicine.medical_specialty
congenital, hereditary, and neonatal diseases and abnormalities
Movement disorders
Encephalopathy
Case Report
Cérébrovasculopathie
puff of smoke
Cerebrovasculopathy
03 medical and health sciences
0302 clinical medicine
bouffée de fumée
medicine.artery
medicine
030212 general & internal medicine
Moyamoya disease
Dystonia
syndrome moyamoya
business.industry
moyamoya syndrome
maladie de moyamoya
General Medicine
medicine.disease
Surgery
nervous system diseases
dystonie
cardiovascular system
Radiology
Neurovascular Disorder
dystonia
Internal carotid artery
medicine.symptom
business
moyamoya disease
Myoclonus
030217 neurology & neurosurgery
Circle of Willis
Subjects
Details
- Language :
- English
- ISSN :
- 09755764 and 15963519
- Volume :
- 15
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Annals of African Medicine
- Accession number :
- edsair.doi.dedup.....ed18a3a4556364a6e6ca0d773d53745c