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Moyamoya Disease and Moyamoya Syndrome
New England Journal of Medicine, 2009Moyamoya disease is a cerebrovascular condition predisposing affected patients to stroke in association with progressive stenosis of the intracranial internal carotid arteries and their proximal branches. Patients with characteristic moyamoya vasculopathy plus associated conditions are categorized as having moyamoya syndrome.
Edward R Smith, Robert Scott
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Pediatric Neurology, 1997 We report a patient with Noonan syndrome and asymptomatic cardiac disease (supravalvular aortic stenosis and pulmonary valvular stenosis) who had frequent transient ischemic attacks. Bilateral moyamoya was evident; in addition, he manifested activated protein C resistance and was heterozygous for the factor V Leiden mutation.
Ganesan, V., Kirkham, F.J.
openaire +4 more sources
Clinical Neurology and Neurosurgery, 1997
Moyamoya disease was first described by Suzuki in 1963. The surgical management of Moyamoya disease began in the mid 1970s. At our institution we began operating on Moyamoya disease in 1979 and between 1979 and 1995 we have treated 30 children with Moyamoya disease and Moyamoya syndrome. Of these 21 children have an excellent outcome.
Harold J Hoffman, H J Hoffman
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Moyamoya disease was first described by Suzuki in 1963. The surgical management of Moyamoya disease began in the mid 1970s. At our institution we began operating on Moyamoya disease in 1979 and between 1979 and 1995 we have treated 30 children with Moyamoya disease and Moyamoya syndrome. Of these 21 children have an excellent outcome.
Harold J Hoffman, H J Hoffman
exaly +3 more sources
Radiation-Induced Moyamoya Syndrome
International Journal of Radiation Oncology Biology Physics, 2006The moyamoya syndrome is an uncommon late complication after radiotherapy (RT).A PubMed search of English-language articles, with radiation, radiotherapy, and moyamoya syndrome used as search key words, yielded 33 articles from 1967 to 2002.The series included 54 patients with a median age at initial RT of 3.8 years (range, 0.4 to 47).
Arnold C Paulino, Bin S Teh
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Management of Moyamoya Syndrome in Patients With Noonan Syndrome
Journal of Clinical Neuroscience, 2016A few isolated reports have described an association between Noonan syndrome and cerebrovascular abnormalities, including moyamoya syndrome. These reports have been limited to pediatric patients presenting with recurrent transient ischemic attacks (TIA) or headaches.
Gerald Grant, Abdullah Feroze
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Stroke, 1996 Background and Purpose Moyamoya disease is a chronic occlusive cerebrovascular disorder characterized by progressive stenosis of the supraclinoid internal carotid artery, with the secondary development of enlarged basal ...
Richard Robertson +2 more
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S.S. Korsakov Journal of Neurology and Psychiatry, 2023
Moyamoya disease (MMD) is a rare disease characterized by progressive stenosis of the terminal part of the internal carotid arteries (ICA) and the proximal part of their branches, which is accompanied by the formation of collateral network that look like smoke clouds on angiography (Japanese terminology — moyamoya).
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Moyamoya disease (MMD) is a rare disease characterized by progressive stenosis of the terminal part of the internal carotid arteries (ICA) and the proximal part of their branches, which is accompanied by the formation of collateral network that look like smoke clouds on angiography (Japanese terminology — moyamoya).
openaire +2 more sources