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Information Journal Paper

Title

Rare Presentation of Moyamoya Disease with Sub acute Presentation in Iran (CASE REPORT)

Pages

  89-93

Abstract

 Moyamoya disease is a chronic progressive vascular disease of brain characterized by bilateral stenosis or occlusion of the arteries around the circle of Willis with prominent arterial collateral circulation. We introduce here a patient with Moyamoya who was misdiagnosed. She was a 16-yrold female from north east of Iran who complained left hemiparesis and was diagnosed Moyamoya disease by brain and cervical CT-Angiography. There was still great difficulty in the diagnosis of diffuse white matter lesions. The CT-Angiography showed bilateral internal carotid stenosis with “ puff of smoke” collateralization arising from the circle of Willis, therefore Moyamoya disease was raised. The clinical diagnosis of Moyamoya is challenging and misdiagnosis is probable. Therefore, the physicians should know this disease and think about it in patients with Juvenile Stroke. This shows that Moyamoya disease should be considered in differential diagnoses especially among young patients presenting with unexplained cerebrovascular syndromes.

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    APA: Copy

    SASANNEJAD, PAYAM, REZAEI, FATEMEH, BIDAKI, REZA, & ZAREPUR, EHSAN. (2018). Rare Presentation of Moyamoya Disease with Sub acute Presentation in Iran (CASE REPORT). IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), 12(1), 89-93. SID. https://sid.ir/paper/303618/en

    Vancouver: Copy

    SASANNEJAD PAYAM, REZAEI FATEMEH, BIDAKI REZA, ZAREPUR EHSAN. Rare Presentation of Moyamoya Disease with Sub acute Presentation in Iran (CASE REPORT). IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)[Internet]. 2018;12(1):89-93. Available from: https://sid.ir/paper/303618/en

    IEEE: Copy

    PAYAM SASANNEJAD, FATEMEH REZAEI, REZA BIDAKI, and EHSAN ZAREPUR, “Rare Presentation of Moyamoya Disease with Sub acute Presentation in Iran (CASE REPORT),” IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), vol. 12, no. 1, pp. 89–93, 2018, [Online]. Available: https://sid.ir/paper/303618/en

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