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Rarer in a Rare

Though moya moya disease is a disease of Asian origin, it is one of the very rare causes of stroke in India. It is a rare disease mainly characterized by progressive cerebrovascular episode due to the slowly progressive stenosis of supraclinoid segment of bilateral internal carotid arteries, the ant...

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Detalles Bibliográficos
Autores principales: Taksande, B, Patil, MM, Banode, P, Deshpande, R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634211/
https://www.ncbi.nlm.nih.gov/pubmed/23634348
http://dx.doi.org/10.4103/2141-9248.109482
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author Taksande, B
Patil, MM
Banode, P
Deshpande, R
author_facet Taksande, B
Patil, MM
Banode, P
Deshpande, R
author_sort Taksande, B
collection PubMed
description Though moya moya disease is a disease of Asian origin, it is one of the very rare causes of stroke in India. It is a rare disease mainly characterized by progressive cerebrovascular episode due to the slowly progressive stenosis of supraclinoid segment of bilateral internal carotid arteries, the anterior and the middle cerebral arteries, and very rarely, posterior cerebral arteries. We hereby report a case of a young female who presented to us with the psychiatric complaints and refractory headache since her childhood. Therefore, we are reporting rarer (headache and neuropsychiatric) manifestations in the rare (moya moya) disease.
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spelling pubmed-36342112013-04-30 Rarer in a Rare Taksande, B Patil, MM Banode, P Deshpande, R Ann Med Health Sci Res Case Report Though moya moya disease is a disease of Asian origin, it is one of the very rare causes of stroke in India. It is a rare disease mainly characterized by progressive cerebrovascular episode due to the slowly progressive stenosis of supraclinoid segment of bilateral internal carotid arteries, the anterior and the middle cerebral arteries, and very rarely, posterior cerebral arteries. We hereby report a case of a young female who presented to us with the psychiatric complaints and refractory headache since her childhood. Therefore, we are reporting rarer (headache and neuropsychiatric) manifestations in the rare (moya moya) disease. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3634211/ /pubmed/23634348 http://dx.doi.org/10.4103/2141-9248.109482 Text en Copyright: © Annals of Medical and Health Sciences Research 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 Case Report
Taksande, B
Patil, MM
Banode, P
Deshpande, R
Rarer in a Rare
title Rarer in a Rare
title_full Rarer in a Rare
title_fullStr Rarer in a Rare
title_full_unstemmed Rarer in a Rare
title_short Rarer in a Rare
title_sort rarer in a rare
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634211/
https://www.ncbi.nlm.nih.gov/pubmed/23634348
http://dx.doi.org/10.4103/2141-9248.109482
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