Alagille syndrome associated with Moyamoya disease
- 1 May 1989
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 33 (1) , 89-91
- https://doi.org/10.1002/ajmg.1320330112
Abstract
A 22‐month‐old girl with the typical manifestations of Alagille syndrome presented with acute right hemiparesis. Cerebral angiographic studies demonstrated the presence of complete occlusion of both internal carotid arteries with the formation of a collateral network of vessels compatible with the diagnosis of Moyamoya disease. This rare association has not been reported previously.Keywords
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