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CASE REPORT
Year : 2015  |  Volume : 4  |  Issue : 3  |  Page : 200-202

Moyamoya disease - A case report from North Western part of India


Department of General Medicine, Jawaharlal Nehru Medical College, Ajmer, Rajasthan, India

Correspondence Address:
Maniram Kumhar
Jeevan Jadav, Gaurav Enclav, Civil Lines, Ajmer - 305 001, Rajasthan
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2278-344X.160901

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Moyamoya disease is a chronic, progressive occlusion of the circle of Willis arteries that leads to the development of characteristic collateral vessels seen on imaging, particularly cerebral angiography. The disease may develop in children and adults, but the clinical features differ. Moyamoya disease occurs predominantly in Japanese individuals but has been found in all races with varying age distributions and clinical manifestations. As a result, moyamoya disease has been under-recognized as a cause of ischemic and hemorrhagic strokes in the Indian subcontinent. At this time, there is no known cure, and existing treatment options are controversial. We here describe the case of a 27-year-old Indian presenting as right-sided hemiparesis with accelerated hypertension.


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