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 CASE REPORT
Year : 2018  |  Volume : 13  |  Issue : 2  |  Page : 245-248

Endovascular treatment of a patient with Moyamoya disease and Seckel syndrome: A case report


1 Department of Radiology, Baskent University, Teaching and Research Center, Adana/TURKEY, Turkey
2 Department of Pediatric Neurology, Baskent University, Teaching and Research Center, Adana/TURKEY, Turkey
3 Department of Neurosurgery, Baskent University, Teaching and Research Center, Adana/TURKEY, Turkey

Correspondence Address:
Aylin Gunesli
Baskent University, Adana Teaching and Research Center, Department of Radiology, Dadaloglu Mh. 2591 Sk. No:4/A PK:01250 Yuregir/ADANA, Turkey
Turkey
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/JPN.JPN_96_17

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Seckel syndrome and Moyamoya diseases are different entities that rarely associated with each other. Several cases presenting with both these diseases were reported. Intracerebral artery aneurysms and collateral vessels can be seen with Moyamoya. They are commonly treated with medical treatment. We present a 12-years old patient with both Seckel syndrome and Moyamoya disease presented with middle cerebral artery aneurysm which was treated with endovascular modalities.






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