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The authors report four cases of familial occurrence of moyamoya disease . Although the pathogenesis of moyamoya disease is not clear, there is extensive evidence that this disease has a tendency ...
Childs Nerv Syst (2006) 22: 1143–1148 DOI 10.1007/s00381-006-0089-4 ORIGINAL PAPER Ho Jun Seol Familial occurrence of moyamoya disease : Kyu-Chang Wang Seung-Ki Kim a clinical study Yong-Seung Hwang ...
Background: There was few detailed demographic and clinical data about Chinese patients with moyamoya disease . Here we describe the clinical features, surgical treatment, and long-term outcome ...
Two out of six siblings with neurofibromatosis (in a sibship of eight) had clinical and roentgenographic evidence of Moyamoya -type, intracranial arterial occlusive disease . This rare vascular ...
disease and eosinophilic granuloma. Although the etiology of moyamoya disease is unknown, a familial pattern of occurrence has been documented. Of particular importance is its presentation with polycystic ...
Among patients with moyamoya disease , familial occurrence is observed in about 20%, suggesting the involvement of genetic factors. In this report, we describe the first predictive case of moyamoya ...
We documented an interesting case of adult “unilateral (probable)” moyamoya disease displaying familial occurrence in two “definite” cases. A 55-year-old female presented with motor aphasia ...
in Japanese and Koreans and approximately 10% of familial occurrence among the Japanese. Recent genetic studies suggest some responsible genetic foci in chromosomes 3, 6 and 17. HISTORY Moyamoya disease ...
Supplemental Digital Content is available in the text. Stroke CLINICAL AND POPULATION SCIENCES Familial Risk for Moyamoya Disease Among First- Degree Relatives, Based on a Population-Based ...
Masuda et al SMC Proliferation in Moyamoya Disease 1967 19. Kitahara Ariga N, Yamamura A, Makino H. A familial T, 24. Yamashita M, Oka K, Tanaka K. Cervico-cephalic arterial thrombi occurrence ...
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