| Literature DB >> 1694272 |
A Ikeda1, I Iguchi, M Hara, I Yamamoto, O Sato.
Abstract
The authors report an instance of familial moyamoya disease involving a 47-year-old female and her 18-year-old daughter, both of whom initially presented, within a 1-year period, with intracranial hemorrhage. Cerebral angiography showed the typical features of moyamoya disease. The mother, whose disease was more advanced, underwent superficial temporal-middle cerebral artery bypass, with satisfactory results. Human leukocyte antigen typing was performed in both cases. The pertinent literature is reviewed.Entities:
Mesh:
Year: 1990 PMID: 1694272 DOI: 10.2176/nmc.30.43
Source DB: PubMed Journal: Neurol Med Chir (Tokyo) ISSN: 0470-8105 Impact factor: 1.742