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Varied presentations of moyamoya disease in a tertiary care hospital of north-east India
INTRODUCTION: Moyamoya disease is a chronic progressive cerebrovascular disorder, characterized by stenosis or occlusion of bilateral internal carotid arteries (ICAs), anterior cerebral arteries (ACAs) and middle cerebral arteries (MCAs), accompanied by a collateral network of vessels formed at the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162020/ https://www.ncbi.nlm.nih.gov/pubmed/25221403 http://dx.doi.org/10.4103/0972-2327.138518 |
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author | Borah, Papori Sharma, Vikas Basumatary, Lakshya Jyoti Das, Marami Goswami, Munindra Kayal, Ashok K. |
author_facet | Borah, Papori Sharma, Vikas Basumatary, Lakshya Jyoti Das, Marami Goswami, Munindra Kayal, Ashok K. |
author_sort | Borah, Papori |
collection | PubMed |
description | INTRODUCTION: Moyamoya disease is a chronic progressive cerebrovascular disorder, characterized by stenosis or occlusion of bilateral internal carotid arteries (ICAs), anterior cerebral arteries (ACAs) and middle cerebral arteries (MCAs), accompanied by a collateral network of vessels formed at the base of the brain. Ischemia and intracranial hemorrhage are the common typical manifestations. However moyamoya disease has been associated with atypical presentations like headache, seizures and involuntary movements. Although frequently reported from Asian countries like Japan, China and Korea, only few studies reported on clinical manifestations of moyamoya disease from India. OBJECTIVES: To study the varied presentations of moyamoya disease in a tertiary care hospital of north-east India. MATERIAL AND METHODS: Relevant investigations were done to rule out other causes of moyamoya syndrome. RESULTS: We report 6 cases of moyamoya disease with varied presentations from a tertiary care referral government hospital. Case 1, 2 and 6 presented with alternating hemiparesis. Case 3 had amaurosis fugax. Case 4 had history suggestive of ischemic stroke and presented with hemichorea. Case 4 had focal seizure as the only manifestation. Cases 4 and 5 notably had stenosis of posterior cerebral artery (PCA) in addition to stenosis of bilateral ICAs, ACAs and MCAs. CONCLUSION: Owing to its low incidence in India, moyamoya disease is easily overlooked as a possible diagnosis. However, because of its progressive nature, it is imperative to diagnose this disease early and offer surgical treatment to the patients. |
format | Online Article Text |
id | pubmed-4162020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41620202014-09-14 Varied presentations of moyamoya disease in a tertiary care hospital of north-east India Borah, Papori Sharma, Vikas Basumatary, Lakshya Jyoti Das, Marami Goswami, Munindra Kayal, Ashok K. Ann Indian Acad Neurol Original Article INTRODUCTION: Moyamoya disease is a chronic progressive cerebrovascular disorder, characterized by stenosis or occlusion of bilateral internal carotid arteries (ICAs), anterior cerebral arteries (ACAs) and middle cerebral arteries (MCAs), accompanied by a collateral network of vessels formed at the base of the brain. Ischemia and intracranial hemorrhage are the common typical manifestations. However moyamoya disease has been associated with atypical presentations like headache, seizures and involuntary movements. Although frequently reported from Asian countries like Japan, China and Korea, only few studies reported on clinical manifestations of moyamoya disease from India. OBJECTIVES: To study the varied presentations of moyamoya disease in a tertiary care hospital of north-east India. MATERIAL AND METHODS: Relevant investigations were done to rule out other causes of moyamoya syndrome. RESULTS: We report 6 cases of moyamoya disease with varied presentations from a tertiary care referral government hospital. Case 1, 2 and 6 presented with alternating hemiparesis. Case 3 had amaurosis fugax. Case 4 had history suggestive of ischemic stroke and presented with hemichorea. Case 4 had focal seizure as the only manifestation. Cases 4 and 5 notably had stenosis of posterior cerebral artery (PCA) in addition to stenosis of bilateral ICAs, ACAs and MCAs. CONCLUSION: Owing to its low incidence in India, moyamoya disease is easily overlooked as a possible diagnosis. However, because of its progressive nature, it is imperative to diagnose this disease early and offer surgical treatment to the patients. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4162020/ /pubmed/25221403 http://dx.doi.org/10.4103/0972-2327.138518 Text en Copyright: © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Borah, Papori Sharma, Vikas Basumatary, Lakshya Jyoti Das, Marami Goswami, Munindra Kayal, Ashok K. Varied presentations of moyamoya disease in a tertiary care hospital of north-east India |
title | Varied presentations of moyamoya disease in a tertiary care hospital of north-east India |
title_full | Varied presentations of moyamoya disease in a tertiary care hospital of north-east India |
title_fullStr | Varied presentations of moyamoya disease in a tertiary care hospital of north-east India |
title_full_unstemmed | Varied presentations of moyamoya disease in a tertiary care hospital of north-east India |
title_short | Varied presentations of moyamoya disease in a tertiary care hospital of north-east India |
title_sort | varied presentations of moyamoya disease in a tertiary care hospital of north-east india |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162020/ https://www.ncbi.nlm.nih.gov/pubmed/25221403 http://dx.doi.org/10.4103/0972-2327.138518 |
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