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Japanese

"Moyamoya" Disease Found in Identical Twins Makoto SONOBE 1 , Shinichiro TAKAHASHI 1 , Yoichi URAKAWA 1 , Yoshihide NAGAMINE 1 , Namio KODAMA 2 , Hitoshi FUKAZAWA 3 1Division of Neurosurgery, Mito National Hospital 2Division of Neurosurgery, Institute of Brain Diseases, Tohoku University School of Medicine 3Division of Pathology, Research Institute of Brain and Blood Vessels Keyword: Identical twins , Moyamoya disease pp.1183-1188
Published Date 1980/12/10
DOI https://doi.org/10.11477/mf.1436201249
  • Abstract
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Congenital anomaly embryonal persistent vessel and/or secondary collateral pathway are thought as an etiology or pathogenesis of Moyamoya Disease (M.M.D.), but the truth is still unknown. Authors have reported here, twins of M.M.D. Pathological findings are examined in an autopsy case. In other case, right hemiparesis and dysphasis is unproved by STA-MCA anastomosis and encephalo-myo synangiosis. In a review of literature of 8 brothers (17 cases), participation of hereditary factors for genesis of M.M.D. are discussed.


Copyright © 1980, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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