A Child with Moyamoya Disease: A Case Report
Cerebral stroke is a rare disease in children. Moyamoya (MM) is one of the infrequent cerebrovascular diseases with unknown etiology. We report an 8 year-old-boy with chief complain of sudden onset bilateral parietal lobe headache. He mentioned that his headache was first started about three weeks a...
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Shahid Beheshti University of Medical Sciences
2015-04-01
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Series: | International Clinical Neuroscience Journal |
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doaj-1a35554b6e6842648ee3ec6658089c1d2020-11-25T01:29:44ZengShahid Beheshti University of Medical SciencesInternational Clinical Neuroscience Journal2383-18712383-20962015-04-0122747610.22037/icnj.v2i2.8924icnj-3061A Child with Moyamoya Disease: A Case ReportFarzad Ashrafi0Behdad Behnam1Hamid Reza Rokhsat Yazdi2Mehran Arab Ahmadi3Payam Sarraf4Functional Neurosurgery Research Center, Shohada Tajrish Hospital, Tajrish Square, Tehran, IranFunctional Neurosurgery Research Center, Shohada Tajrish Hospital, Tajrish Square, Tehran, IranFunctional Neurosurgery Research Center, Shohada Tajrish Hospital, Tajrish Square, Tehran, IranFunctional Neurosurgery Research Center, Shohada Tajrish Hospital, Tajrish Square, Tehran, IranFunctional Neurosurgery Research Center, Shohada Tajrish Hospital, Tajrish Square, Tehran, IranCerebral stroke is a rare disease in children. Moyamoya (MM) is one of the infrequent cerebrovascular diseases with unknown etiology. We report an 8 year-old-boy with chief complain of sudden onset bilateral parietal lobe headache. He mentioned that his headache was first started about three weeks ago and was associated with visual disturbance. His mother declared that the boy developed gait problems few days later and only could walk with assistance. He was diagnosed with MM disease. After, medical treatment his symptoms were mildly improved and because of his family disagreement cerebral revascularization surgery was not performed.http://journals.sbmu.ac.ir/Neuroscience/article/download/8924/pdf_22 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Farzad Ashrafi Behdad Behnam Hamid Reza Rokhsat Yazdi Mehran Arab Ahmadi Payam Sarraf |
spellingShingle |
Farzad Ashrafi Behdad Behnam Hamid Reza Rokhsat Yazdi Mehran Arab Ahmadi Payam Sarraf A Child with Moyamoya Disease: A Case Report International Clinical Neuroscience Journal |
author_facet |
Farzad Ashrafi Behdad Behnam Hamid Reza Rokhsat Yazdi Mehran Arab Ahmadi Payam Sarraf |
author_sort |
Farzad Ashrafi |
title |
A Child with Moyamoya Disease: A Case Report |
title_short |
A Child with Moyamoya Disease: A Case Report |
title_full |
A Child with Moyamoya Disease: A Case Report |
title_fullStr |
A Child with Moyamoya Disease: A Case Report |
title_full_unstemmed |
A Child with Moyamoya Disease: A Case Report |
title_sort |
child with moyamoya disease: a case report |
publisher |
Shahid Beheshti University of Medical Sciences |
series |
International Clinical Neuroscience Journal |
issn |
2383-1871 2383-2096 |
publishDate |
2015-04-01 |
description |
Cerebral stroke is a rare disease in children. Moyamoya (MM) is one of the infrequent cerebrovascular diseases with unknown etiology. We report an 8 year-old-boy with chief complain of sudden onset bilateral parietal lobe headache. He mentioned that his headache was first started about three weeks ago and was associated with visual disturbance. His mother declared that the boy developed gait problems few days later and only could walk with assistance. He was diagnosed with MM disease. After, medical treatment his symptoms were mildly improved and because of his family disagreement cerebral revascularization surgery was not performed. |
url |
http://journals.sbmu.ac.ir/Neuroscience/article/download/8924/pdf_22 |
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